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Clinic-Grade Laser and RF Devices: Complete Guide for Safe, Effective Results

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Clinic-grade laser and radiofrequency devices are professional energy-based systems used by medical and aesthetic practitioners to treat skin, hair, and body concerns with controlled light and heat. Understanding what makes a device truly clinic-grade is essential for clinics, med spas, dermatology practices, and patients who want safe, predictable outcomes and a strong return on investment.

What Are Clinic-Grade Laser Devices?

Clinic-grade laser devices are medical or aesthetic systems that emit focused light at specific wavelengths to target structures in the skin or hair while sparing surrounding tissue. They are typically classified as medical devices, require regulatory clearance, and must be operated by trained professionals or under physician supervision. In practice, these devices are used for laser hair removal, skin resurfacing, pigmentation, vascular lesions, acne scarring, tattoo removal, and scar revision.

Key elements that define clinic-grade laser equipment include stable energy delivery, precise fluence control, adjustable pulse durations, and advanced cooling for epidermal protection. They are built for continuous or high-frequency use in busy clinics, equipped with robust handpieces, integrated monitoring, and safety interlocks. Compared with consumer laser gadgets, professional laser platforms reach higher energy levels, wider parameter ranges, and deeper penetration needed for consistent results on diverse skin types and indications.

What Are Clinic-Grade RF Devices?

Clinic-grade radiofrequency devices deliver controlled electrical energy into the skin or subcutaneous tissue to generate heat and stimulate collagen, elastin, and tissue tightening. Unlike lasers, RF is not dependent on chromophores or pigment and can be used safely across all Fitzpatrick skin types when properly configured. These devices are widely used for non-surgical skin tightening, wrinkle reduction, facial contouring, body contouring, cellulite reduction, and post-pregnancy skin laxity.

Professional RF systems include monopolar, bipolar, multipolar, and fractional RF configurations, and may combine RF with microneedling, vacuum suction, ultrasound, or optical energy. Clinical-grade designs incorporate temperature monitoring, impedance tracking, and real-time feedback to maintain optimal therapeutic heating while minimizing burns, discomfort, or downtime. For busy practices, RF devices also offer customizable treatment protocols, multiple applicators, and maintenance programs tailored for high patient throughput.

How Clinic-Grade Devices Differ from Consumer Devices

The gap between clinic-grade laser and RF devices and at-home devices is wide in terms of power, control, and clinical evidence. Consumer devices are typically restricted to lower energy levels, narrower parameter settings, and smaller spot sizes to meet safety regulations for unsupervised use. This often translates into slower results, limited indications, and higher reliance on frequent home sessions.

Clinic-grade devices, on the other hand, are engineered for high power output, large treatment areas, and optimized pulse structures that can reach therapeutic thresholds in fewer sessions. They undergo more extensive testing, are supported by peer-reviewed data or large case series, and usually come with validated protocols for different skin types and concerns. For practices, this difference in capability directly affects treatment times, pricing, and how quickly patients see visible improvements, which ultimately influences satisfaction, retention, and word-of-mouth growth.

Market Trends for Clinic-Grade Laser and RF Devices

The global energy-based aesthetic devices market encompassing clinic-grade laser and RF platforms has been expanding steadily, driven by demand for non-surgical cosmetic procedures, rising disposable income, and social media visibility of skin and body treatments. Recent market research reports indicate that energy-based aesthetic devices, including lasers, radiofrequency, IPL, ultrasound, and combination platforms, are projected to grow at a high single-digit to low double-digit compound annual growth rate over the next five to ten years, with North America currently dominant and Asia-Pacific growing fastest.

Radiofrequency-based aesthetic devices, in particular, are seeing robust growth as patients seek non-invasive skin tightening, facial contouring, and cellulite reduction without surgery. Reports from industry analysts describe the RF aesthetic device market rising from the mid one-billion-dollar range in the mid-2020s to several billions by the early 2030s, supported by expanding med spa networks, technological innovations such as fractional RF and RF microneedling, and increasing acceptance of maintenance-based anti-aging treatments. Laser platforms for hair removal, pigmentation, vascular lesions, and resurfacing remain staples, but RF-based technologies are increasingly chosen for skin laxity and texture concerns.

Core Technologies in Clinic-Grade Laser Devices

Clinic-grade laser devices are defined by their wavelengths, pulse characteristics, delivery systems, and cooling technologies. Key categories include:

  • Alexandrite lasers, typically around 755 nm, widely used for hair removal on lighter skin types and certain pigmented lesions.

  • Diode lasers for hair removal, often in the 800–810 nm range, with high fluence and large spot sizes to treat large body areas efficiently.

  • Nd:YAG lasers, commonly 1064 nm, used for hair removal in darker skin types, vascular lesions, and deeper dermal targets.

  • CO2 lasers at 10,600 nm and Er:YAG lasers near 2940 nm for ablative and fractional resurfacing, treating wrinkles, acne scars, and textural irregularities.

  • Picosecond and Q-switched lasers for tattoo removal and stubborn pigmentation.

Clinic-grade platforms combine these wavelengths with scanned delivery, fractional patterns, and various pulse structures to balance efficacy and downtime. For example, fractional CO2 and fractional Er:YAG create microthermal zones that encourage rapid healing while improving fine lines and scars. Long-pulsed Nd:YAG systems offer deeper penetration for leg veins and thick hair, while advanced cooling technologies such as cryogen spray, contact sapphire tips, or air cooling reduce risk of burns and hyperpigmentation.

Core Technologies in Clinic-Grade RF Devices

Clinic-grade radiofrequency devices rely on electrical resistance of tissue to generate controlled thermal injury for remodeling and tightening. The main technological variations include:

  • Monopolar RF, where current flows from a small active electrode to a distant grounding pad, allowing deeper volumetric heating used for skin tightening and some body contouring.

  • Bipolar and multipolar RF, where current flows between two or more closely spaced electrodes, creating more confined, controllable heating primarily in the dermis.

  • Fractional RF, often delivered via microneedles or pins, where RF energy is emitted through a matrix of tiny electrodes that create microscopic zones of thermal coagulation and neocollagenesis.

  • RF microneedling, combining mechanical microinjury with RF heating at precise depths, used for acne scars, wrinkles, and skin laxity.

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Modern clinic-grade RF systems incorporate real-time temperature monitoring, impedance feedback, and algorithm-driven energy adjustments to keep tissue within a target temperature range associated with collagen denaturation and subsequent remodeling. Treatment endpoints such as patient-reported heat, visible erythema, and target surface temperature are used to gauge adequate dosing while minimizing pain or complications. Multimodal platforms integrate RF with ultrasound, IPL, or laser to address multiple layers and concerns in a single session.

Safety Standards and Regulatory Considerations

Clinic-grade laser and RF devices are subject to regulatory oversight, which varies by region but typically includes classification as medical devices with specific safety and performance standards. In the United States, devices generally require clearance or approval from the Food and Drug Administration for specific indications such as hair removal, wrinkle reduction, or treatment of acne scars. In Europe, devices must comply with regulations and carry appropriate CE marking, while other regions have their own regulatory agencies and requirements.

Safety frameworks usually cover electrical safety, electromagnetic compatibility, optical radiation safety, labeling, and user manuals. Many clinic-grade systems incorporate hardware and software interlocks, emergency stop features, handpiece recognition, and self-diagnostic functions. Clinics are expected to maintain detailed logs of device maintenance, calibrations, and service events. Practitioners must be trained on laser and RF safety principles, including eye protection, plume management for ablative lasers, grounding pad placement for monopolar RF, and proper parameter selection based on skin type and indication.

Indications and Treatment Applications

Clinic-grade laser and RF devices serve a wide range of aesthetic and dermatologic applications. Common uses include:

  • Laser hair removal on face and body, with diode, alexandrite, and Nd:YAG systems tailored to different hair and skin types.

  • Non-ablative and ablative resurfacing for fine lines, wrinkles, acne scars, and photoaging using fractional CO2, Er:YAG, or non-ablative fractional lasers.

  • Pigmentation treatments for lentigines, melasma management strategies, and post-inflammatory hyperpigmentation with appropriate settings and wavelengths.

  • Vascular lesion treatment such as telangiectasias, facial redness, leg veins, and certain birthmarks.

  • RF-based skin tightening of the face, neck, jawline, abdomen, arms, and thighs.

  • RF or combined RF and ultrasound body contouring and cellulite reduction.

  • RF microneedling for texture, pores, acne scars, and skin laxity, particularly in patients seeking lower downtime than ablative lasers.

Combined treatment plans often pair laser resurfacing with RF tightening or pigment correction with RF microneedling to address multiple dimensions of aging in a staged or layered approach. Optimizing treatment mapping and spacing sessions appropriately is key to maximizing outcomes and minimizing risk.

Combining Laser and RF in Integrated Platforms

A major trend in clinic-grade systems is integrating multiple energy modalities into single platforms. Some devices combine IPL, diode laser, and RF for hair removal and skin rejuvenation; others merge fractional RF with fractional laser to target both epidermal clarity and dermal tightening. These hybrid or multimodal designs help practices provide comprehensive treatments without purchasing multiple standalone units, improving space utilization and capital efficiency.

Combination protocols use synergistic effects: for example, using RF tightening to address skin laxity and then performing fractional laser resurfacing to refine texture, or combining RF microneedling with low-fluence pigment lasers for acne scarring and dyschromia. When protocols are properly sequenced and dosed, the result is greater perceived improvement with manageable downtime, which can justify premium pricing and package-based models.

Market Demand by Practice Type

Demand for clinic-grade laser and RF devices spans dermatology clinics, plastic surgery centers, medical spas, gynecology practices, and multi-specialty clinics. Dermatology and plastic surgery practices often prioritize high-end fractional lasers, RF microneedling, and combination platforms that support scar revision, resurfacing, and perioperative optimization. Medical spas frequently favor high-throughput hair removal lasers and RF body contouring devices to tap into high-volume services.

Gynecology and urology practices have also adopted specialized RF and laser systems for intimate wellness and pelvic floor applications, expanding the market for energy-based devices beyond traditional cosmetic indications. Multi-specialty groups may centralize devices in shared procedure suites, using scheduling software to maximize utilization. Across all segments, trends toward subscription-based treatment memberships, monthly maintenance sessions, and bundled treatment plans increase recurring revenue from energy-based device procedures.

Real-World Outcomes and ROI for Clinics

From a business perspective, clinic-grade laser and RF devices are capital investments that must generate predictable revenue and profit. Practices typically evaluate devices based on several ROI drivers: procedure fee per session, number of sessions in a treatment package, number of treatable indications, average monthly device utilization, and operational costs such as consumables, service contracts, and staff time. Many clinics benefit from devices that deliver visible improvements in three to six sessions, allowing providers to structure treatment packages that fit common budget ranges.

Quantitatively, a busy med spa might schedule multiple laser hair removal or RF tightening sessions per day, with each treatment room capable of generating several thousand dollars in daily revenue when well utilized. Over the course of a year, a single high-performing device can produce revenue several times its acquisition cost if marketing, patient education, and scheduling are optimized. Practices frequently report that multi-application platforms accelerate breakeven since the same device supports multiple procedures across face and body.

Patient Experience and Comfort

Patient comfort is central to the adoption of clinic-grade laser and RF devices. The latest systems emphasize ergonomic handpieces, integrated cooling, adjustable energy steps, and intelligent pulse patterns that distribute heat more evenly. Proper pre-treatment counseling, topical anesthetics for certain procedures, and techniques such as stacking pulses with monitoring patient feedback help maintain tolerable discomfort levels while still reaching effective tissue temperatures.

Visible improvements such as smoother texture, reduced hair, tightened jawlines, and more uniform tone support positive patient perception. Many practices set expectations that collagen remodeling and tightening processes continue for several months after a series of treatments. Photos taken at baseline and at each follow-up help patients see incremental improvements that they may not notice in daily life, reinforcing the value of continuing treatment plans and future maintenance.

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Clinic-Grade Laser Device Examples and Use Cases

While specific brand names vary by region, clinic-grade laser systems can be grouped into use-case categories:

  • Dedicated hair removal platforms with large-spot diode or alexandrite lasers, ideal for high-volume body hair reduction on legs, back, and underarms.

  • Multi-platform systems that host Nd:YAG, pulsed dye, and other modules for vascular lesions, pigmentation, and some hair removal in darker skin types.

  • Fractional CO2 and Er:YAG systems used for deep resurfacing of acne scars, wrinkles around the eyes and mouth, and overall photodamage.

  • Picosecond and Q-switched platforms deployed for multi-color tattoo removal and stubborn pigmented lesions.

In real clinics, a typical use case might involve a series of four to six fractional CO2 sessions spaced several weeks apart for patients with acne scarring, often paired with pigment lasers for post-inflammatory hyperpigmentation. Another scenario is a hair removal program with six to eight diode sessions for dark hair on light skin, followed by annual touch-ups. These structured protocols are built on clinic-grade devices capable of reproducible parameter settings and stable energy delivery across sessions.

Clinic-Grade RF Device Examples and Use Cases

Clinic-grade RF devices are equally versatile. Common categories include:

  • Monopolar RF systems for non-surgical facial tightening and body skin tightening, often used on the neck, abdomen, and thighs.

  • Multipolar RF and vacuum-assisted platforms for cellulite reduction, circumferential reduction, and localized fat smoothing.

  • Fractional RF microneedling systems targeting fine lines, enlarged pores, acne scars, and mild to moderate skin laxity on the face and neck.

  • RF-based intimate wellness devices designed for tissue tightening and comfort in gynecologic indications.

In everyday practice, a dermatologist might use RF microneedling to treat acne scars on the cheeks with a series of three to four sessions, each tailored with variable needle depth and energy levels. A med spa might focus on RF body tightening packages for postpartum abdominal laxity or upper arm sagging, bundling sessions into three- or six-treatment programs that align with collagen remodeling timelines. These use cases show how clinic-grade RF platforms support different price points and patient goals.

Technology Comparison: Laser vs RF for Clinics

Many clinics weigh whether to invest first in laser or RF technology. The choice depends on patient demographics, regional demand, and existing service lines. Lasers excel in hair removal, pigmentation, vascular lesions, and textural resurfacing, making them foundational for most aesthetic practices. RF technologies shine in skin tightening, body contouring support, and collagen remodeling for patients who may not want ablative resurfacing.

In terms of downtime, non-ablative laser and RF treatments often have minimal recovery, while ablative laser resurfacing can require several days of healing. Profit per hour can be high for hair removal and RF body treatments due to efficient session times and relatively straightforward protocols. Many successful clinics aim to own both laser and RF platforms, using them complementarily to construct full-face and full-body treatment pathways that meet patient expectations across age groups.

Competitor Comparison Matrix: Key Features to Consider

When evaluating clinic-grade laser and RF devices, clinics often compare several dimensions to identify the best fit for their business model. Important features typically assessed include:

  • Power output and range of energy settings for flexibility across indications.

  • Wavelengths or RF configurations and ability to treat diverse skin types, including darker Fitzpatrick categories.

  • Treatment speed driven by spot size, repetition rate, and ergonomics.

  • Integrated cooling or temperature control for comfort and safety.

  • Number and type of handpieces for face, body, and specialized areas.

  • Software features such as preset protocols, user profiles, and data logging.

  • Cost structure, including purchase price, financing options, consumables, and service contracts.

A structured matrix comparing these dimensions across leading platforms helps practices align device characteristics with their patient mix and revenue objectives. For example, a clinic with strong demand for hair removal might prioritize fast diode lasers with large spot sizes, whereas a facial rejuvenation center may favor fractional lasers and RF microneedling.

Total Cost of Ownership and Service Considerations

Total cost of ownership for clinic-grade laser and RF devices goes beyond the sticker price. Practices must account for service contracts, handpiece refurbishments, consumable tips or cartridges, coolant, and potential downtime. Choosing reliable devices with robust after-sales support and transparent maintenance schedules reduces risk of unexpected costs and lost revenue.

Some clinics prefer flexible arrangements such as scaled service levels, pay-per-use consumables, or extended warranties. Resale value and opportunities to trade up to next-generation technology also influence long-term economics. Practices benefit from carefully modeling revenue potential against ongoing costs to determine realistic payback periods, which often range from 12 to 36 months depending on utilization and pricing.

At this point, it is worth noting that ALLWILL is redefining B2B medical aesthetics by focusing on innovative sourcing, maintenance, and upgrade pathways for clinic-grade laser and RF devices. By combining a Smart Center for inspection and refurbishment with brand-agnostic consultations and a structured vendor ecosystem, ALLWILL aims to reduce friction, risk, and cost for practitioners who need reliable devices and long-term support.

Training, Protocols, and Clinical Governance

Owning clinic-grade devices without robust training and protocols undermines both outcome quality and safety. Clinics should establish training pathways for physicians, nurses, and aestheticians that cover device physics, skin assessment, contraindications, troubleshooting, and emergency response. Many manufacturers offer initial and advanced training, but clinics are advised to supplement these with internal protocols and periodic refreshers.

Standard operating procedures should define parameter ranges for specific indications, pre- and post-treatment care, documentation standards, and incident reporting. Clinical governance structures, such as a medical director or advisory committee, ensure that devices are used in line with evidence-based practice and local regulations. Clear consent forms, patient education materials, and realistic expectation setting are essential parts of a safe and efficient treatment ecosystem.

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Real User Cases and Quantified Benefits

Real-world case examples illustrate how clinic-grade laser and RF devices transform both patient outcomes and clinic performance. For instance, a dermatology clinic that adds a fractional resurfacing laser might see significant demand from patients with acne scars and advanced photoaging, leading to higher revenue per patient compared with basic cosmetic consults. Packages that combine fractional laser sessions with supportive skincare can increase per-patient revenue while improving satisfaction.

Similarly, a med spa introducing RF body tightening can market non-surgical contouring and skin laxity programs that appeal to postpartum or weight-loss patients. As treatment series progress, patients often perceive improved firmness, smoother contours, and better skin quality, making them more likely to enroll in maintenance plans and refer friends. Over the course of a year, the cumulative effect of higher ticket services and recurring visits can meaningfully improve clinic profitability.

Selection Criteria for New Buyers

For clinics evaluating their first or next clinic-grade laser or RF device, several practical questions guide decision-making:

  • Which treatments are most in demand among current patients, and which new services could reasonably be marketed?

  • What is the typical spending capacity of the patient base, and how does it align with treatment package pricing?

  • How much physical space and electrical capacity does the clinic have for new equipment?

  • Will the primary users be physicians, nurses, or aestheticians, and what level of training can be supported?

  • Is the clinic prepared to invest in marketing campaigns to promote the new services?

Answering these questions before selecting a device prevents mismatches between technology capabilities and real-world utilization. A device that aligns with local demographics and existing skill sets is more likely to be used heavily, accelerating payback and justifying future technology upgrades.

Future Trends in Clinic-Grade Laser and RF Devices

The future of clinic-grade laser and RF devices will likely be shaped by several intersecting trends. First, personalization is increasing as devices incorporate AI-driven parameter recommendations, skin analyzers, and imaging that help tailor treatments to individual skin conditions and goals. Second, combination platforms that merge multiple energies in single passes or staged protocols are becoming more sophisticated, aiming for better results with less downtime.

Third, compact and modular systems are gaining appeal as clinics seek flexible devices that can be upgraded with new handpieces or software instead of replacing entire platforms. Fourth, emphasis on safety and inclusivity is driving innovation for treating darker skin types and sensitive areas without compromising efficacy. Finally, integration with digital practice management systems and remote monitoring may allow providers to track outcomes, schedule reminders, and manage service events for devices more efficiently.

Frequently Asked Questions About Clinic-Grade Laser and RF Devices

1) What makes clinic grade laser and RF devices safe and effective for practice growth?
Acknowledge safety protocols, calibration standards, and validation testing. Prioritize devices with rigorous safety certifications, routine maintenance plans, and operator training to ensure consistent results and minimize downtime. ALLWILL offers refurbished options with full condition reports and warranty coverage to support reliable performance.

2) How can practitioners evaluate long-term cost efficiency of laser and RF devices?
Consider total cost of ownership: purchase price, maintenance, consumables, and downtime. Compare refurbished versus new options, assess warranty terms, and leverage trade-up programs to access newer tech without heavy upfront costs. ALLWILL provides transparent cost analyses and devices aligned to budget and outcomes.

3) Which post-purchase services maximize uptime for clinic devices?
Rely on dealer-backed service networks, scheduled preventive maintenance, and quick-repair capabilities. Ensure access to certified technicians, remote diagnostics, and dependable parts supply. ALLWILL’s Smart Center and MET ensure rapid inspection, repair, and trained support whenever needed.

4) How should clinics approach device training for staff efficiency?
Mandate hands-on training with manufacturers’ protocols, plus ongoing competency assessments. Prefer vendors offering in-house trainers and validated curricula. ALLWILL connects clients to vetted trainers and comprehensive education through its vendor management system.

5) What are key considerations when selecting a device for transactional upgrades?
Look for upgrade paths, compatibility with existing platforms, and favorable trade-in terms. Favor flexible financing or trade-up options that minimize recertification fees. ALLWILL facilitates brand-agnostic consultations and upgrade pathways to stay current.

6) How can clinics verify device performance before purchase?
Request performance reports, calibration records, and refurbished unit warranties. Seek independent third-party verification of outputs and safety checks. ALLWILL provides thorough device inspections and performance guarantees through its processing facilities.

7) What indicators show a device is suitable for a busy aesthetics practice?
High reliability, fast treatment cycles, minimal downtime, and straightforward maintenance. Verify available on-site service, spare parts, and operator-friendly interfaces. ALLWILL emphasizes efficiency, data-driven decisions, and scalable solutions for growing clinics.

8) How can clinics ensure compliant use of laser and RF devices?
Adhere to local regulations, operator certification, and documented safety protocols. Maintain logs of maintenance, inspections, and training. ALLWILL supports compliance through transparent records and access to trained professionals.

Conversion-Focused Next Steps for Clinics

Clinics considering clinic-grade laser and RF devices can start by defining their ideal patient journey and mapping which treatments add the most value at each stage, from prevention and early maintenance to correction and long-term optimization. Once goals are clear, practices can shortlist technologies that match their patient mix, staff expertise, and space, then engage with reputable vendors or independent advisors to compare platforms, service models, and financing options.

After selecting a device, practices should invest in team training, build treatment menus and pricing structures, and create educational content that explains treatments in simple, reassuring language for patients. Launch campaigns, early-bird promotions for existing clients, and structured before-and-after photo protocols help generate early momentum. By aligning technology choice, clinical protocols, patient communication, and marketing strategy, clinics can unlock the full potential of clinic-grade laser and RF devices and build sustainable, high-value service lines that grow year after year.

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(b) Special Order Product. If this Agreement includes the sale of a product that MRP does not currently have or typically keep in stock, in MRP’s sole determination, but is acquired from a third party specifically for Buyer (a “Special Order Product”), then Buyer agrees that (i) Buyer, at its sole discretion, has made the selection of such Special Order Product, (ii) such Special Order Product is being acquired by MRP solely at the request of Buyer, (iii) no representation, warranty or guarantee has been made by MRP with respect to such Special Order Product, (iv) the obligation of Buyer to pay MRP for the Special Order Product is absolute and unconditional, and (v) Buyer waives and releases MRP from all claims, damages and losses arising out of such Special Order Product. Special Order Products carry no right to inspection before or after delivery, and MRP is not responsible for examining or evaluating such Special Order Products. MRP makes no warranty about Special Order Products and offerings of the third party (including description of the Special Order Product). MRP does not assume any responsibility or liability for the actions, product and content of all these and any other third parties. If there are any problems with any Special Order Product, Buyer must contact the manufacturer of such Special Order Product for assistance.

(c) Limited Warranties, If Any.

(i) If the Quote expressly states that the Equipment has a warranty for a certain time (a “Warranty Period”), then MRP warrants that the Equipment shall be in good working order under normal use for the Warranty Period, which Warranty Period shall commence from the date of delivery to Buyer (the “Delivery Date”), unless otherwise approved by an MRP Officer in writing, except for the following: (A) New (not used or pre-owned) Equipment that is to be serviced by MRP: if the Quote is silent, warranted to be in good working order under normal use for one hundred eighty (180) days from the Delivery Date; (B) Used Equipment sold refurbished by MRP: if the Quote is silent, warranted to be in good working order under normal use for thirty (30) days from the Delivery Date; (C) Consumable/disposable Equipment: if the Quote is silent, warranted to have been shipped from MRP in functional condition, and no additional warranty shall apply; no service shall be provided either. These items should be inspected for obvious damage, subject to Section 6 and 8(e), and MRP’s obligation under this warranty and this Section 8(c)(i)(C) is limited to replacement of the Equipment; and (D) New (not used or pre-owned) Equipment that is to be serviced by the manufacturer: if the Quote is silent, MRP makes no warranty for any such Equipment. Buyer’s sole warranty for any such Equipment, if any, shall be the original manufacturer’s warranty, which MRP agrees to pass on to Buyer, as applicable. (ii) For the limited warranties of Section 8(c)(i), including exceptions (A) and (B), but not (C) or this (D), Buyer is entitled to telephone, e-mail and video technical assistance and, subject to Sections 8(d) and 8(e), repair or replacement of such Equipment, in MRP’s sole discretion, should the Equipment become inoperative through normal use during the Warranty Period. Loaner equipment is not provided, but if so arranged by MRP, Buyer shall pay MRP the cash list price of any unreturned loaner equipment provided by MRP within seven (7) days of a written demand from MRP. (iii) Repair or replacement under any limited warranty of Equipment may be with parts or products that are new, used or refurbished, carrying the same limited warranty for the remaining term of the original item. Repairs or replacements shall not interrupt, extend or prolong the term of the warranty. (iv) For Services purchased under this Agreement, MRP warrants that the Services shall be performed using competent personnel in a professional manner in accordance with generally recognized industry standards for similar services. Subject to Sections 6 and 8(e) herein, if any Service was not performed in accordance with the aforementioned warranty, then MRP shall, in its sole discretion, either (A) repair or re-perform the applicable Service, or (B) credit or refund the price of such Service at the pro rata contract rate.

(d) Exclusions. MRP reserves the right, without liability, to void all warranties and remedies, including any obligation to service, repair, replace or otherwise remedy defects, errors or failures of the Equipment due to the occurrence of any of these events, and MRP shall be in no way responsible for: (i) handling, maintenance or use in a manner that is inconsistent with and/or contrary to the original manufacturer’s or MRP’s recommended procedures and/or instructions, including, without limitation, use of or with an unauthorized third-party good or part; (ii) any failure or damage resulting from negligence, alteration, modification or relocation of the Equipment by Buyer, its employees, agents or representatives; (iii) attempted or actual unauthorized dismantling, disassembling, service, repair, addition or change of the Equipment, including, without limitation, changing the serial number or shot count; (iv) abnormal wear and tear, including, without limitation, use under abnormal conditions (e.g., unclean, dusty, or exposure to extreme electromagnetic radiation, temperature or humidity); or (v) damage or failure of the Equipment due to a Force Majeure Event or a problem in the premises of the Equipment. In any of the above situations, or for any Equipment that has no warranty, MRP has sole discretion to service the Equipment, at Buyer’s expense, at MRP’s then-in-effect rates for service, labor, travel, shipping and materials.

(e) Notice and Inspection. The limited warranties contained in this Section 8 are made on condition that immediate written notice of any noncompliance with the Equipment’s and/or the Service’s warranty be given to MRP, and provided that MRP’s inspection reveals that Buyer’s claim is valid under the terms of such warranty.

        9.  DISCLAIMERS; NO OTHER WARRANTY. EXCEPT TO THE EXTENT AS PROVIDED IN SECTION 8(c)(i)(D), BUYER ACKNOWLEDGES THAT MRP IS NOT BOUND BY ANY WARRANTY THAT MAY BE SET FORTH IN A MANUFACTURER’S WRITTEN MATERIALS THAT WOULD HAVE APPLIED HAD BUYER PURCHASED THE EQUIPMENT DIRECTLY FROM THE MANUFACTURER IN ITS UNUSED STATE. BUYER ACKNOWLEDGES THAT BUYER HAS NOT RELIED UPON ANY WARRANTY OTHER THAN AS SET FORTH IN THIS AGREEMENT. IN ADDITION, BUYER ALSO HEREBY ACKNOWLEDGES AND AGREES THAT ANY ORAL OR WRITTEN STATEMENTS CONCERNING USE AND REGULATION OF MEDICAL DEVICES SOLD BY MRP ARE AND SHALL BE CONSTRUED AS FOR INFORMATIONAL PURPOSES ONLY AND WITHOUT WARRANTY OR ASSURANCE BY MRP AS TO THEIR ACCURACY OR VALIDITY. MRP ALSO HEREBY DISCLAIMS ANY AND ALL WARRANTIES REGARDING OTHER MEDICAL CARE OR HELP, INCLUDING THE SELECTION OF AESTHETIC AND MEDICAL PROCEDURES AND PRODUCTS FOR, OR CARE OF, PATIENTS. THE LIMITED WARRANTIES OF THIS AGREEMENT, IF APPLICABLE TO ANY EQUIPMENT OR SERVICE FURNISHED UNDER THIS AGREEMENT, CONSTITUTE THE ONLY WARRANTIES MADE WITH RESPECT TO THE EQUIPMENT AND/OR SERVICE AND ANY DEFECT, DEFICIENCY OR NONCONFORMITY. TO THE EXTENT PERMITTED BY LAW, SUCH WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESS OR IMPLIED BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE, INCLUDING, BUT NOT LIMITED TO, ANY EXPRESS OR IMPLIED WARRANTY OF MERCHANTABILITY, TITLE, NONINFRINGEMENT OR FITNESS FOR A PARTICULAR PURPOSE.

        10.  LIMITATION OF LIABILITY. NOTWITHSTANDING ANYTHING TO THE CONTRARY IN THIS AGREEMENT, UNDER NO CIRCUMSTANCES SHALL MRP BE LIABLE FOR ANY INDIRECT, PUNITIVE, INCIDENTAL, CONSEQUENTIAL, EXEMPLARY OR SPECIAL DAMAGES, ARISING FROM, RELATED TO OR CAUSED, DIRECTLY OR INDIRECTLY, WHETHER FORESEEABLE OR NOT, BY THE EQUIPMENT AND/OR THE SERVICES, THE USE OR INABILITY TO USE THE EQUIPMENT, THE RESULTS GENERATED FROM THE EQUIPMENT AND/OR THE SERVICES, THIS AGREEMENT, ANY OTHER ACT OR OMISSION OF MRP, OR BASED UPON ANY OTHER LEGAL THEORY. IN NO EVENT SHALL MRP BE LIABLE FOR ANY LOSSES OF REVENUE, USE, BUSINESS OPPORTUNITY, PROFIT, SAVINGS OR ANY OTHER DAMAGES DUE TO ANY CAUSE WHATSOEVER, EVEN IF MRP OR ITS AGENTS HAS BEEN ADVISED OF THE POSSIBILITY THEREOF. THE FOREGOING IS A SEPARATE, ESSENTIAL TERM OF THIS AGREEMENT, AND SHALL BE EFFECTIVE UPON THE FAILURE OF ANY REMEDY, EXCLUSIVE OR NOT. IN NO EVENT WILL MRP’S TOTAL LIABILITY UNDER THIS AGREEMENT EXCEED THE PURCHASE PRICE ACTUALLY PAID TO MRP BY BUYER FOR THE EQUIPMENT AND/OR THE SERVICES GIVING RISE TO THE CLAIM FOR WHICH DAMAGES ARE BEING SOUGHT. NO SUIT OR ACTION MAY BE BROUGHT BY BUYER, ITS SHAREHOLDERS, DIRECTORS, MANAGERS, EMPLOYEES OR AGENTS FOR ANY BREACH OF THIS AGREEMENT MORE THAN ONE (1) YEAR AFTER THE ACCRUAL OF SUCH CAUSE OF ACTION. IT IS AGREED THAT MRP’S LIABILITY IS SO LIMITED. WITHOUT LIMITING THE GENERALITY OF THE FOREGOING, BUYER ASSUMES ALL RISK AND LIABILITY FOR THE RESULTS OBTAINED BY THE USE OF ANY EQUIPMENT IN THE PRACTICE OF ANY PROCESS, WHETHER IN TERMS OF OPERATING COSTS, GENERAL EFFECTIVENESS, SUCCESS OR FAILURE, AND REGARDLESS OF ANY ORAL OR WRITTEN STATEMENTS MADE BY MRP, BY WAY OF TECHNICAL ADVICE OR OTHERWISE, RELATED TO THE USE OF THE EQUIPMENT.

        11.  BUYER’S REPRESENTATIONS AND WARRANTIES. Buyer represents and warrants to MRP that: (a) Buyer is duly organized, validly existing, and in good standing in the jurisdiction of Buyer’s formation; (b) Buyer is duly qualified to do business and is in good standing in every jurisdiction in which such qualification is required; (c) Buyer has the full right, power, and authority to enter into this Agreement and to perform Buyer’s obligations under this Agreement; (d) the execution of this Agreement by the person whose signature is set forth at the end hereof has been duly authorized by all necessary corporate action of Buyer; (e) when executed and delivered by each of MRP and Buyer, this Agreement will constitute the legal, valid and binding obligation of Buyer, enforceable against Buyer in accordance with its terms; (f) Buyer is in compliance with all applicable laws relating to this Agreement, the Equipment and the operation of Buyer’s business; (g) Buyer is not insolvent and is paying all of its debts as they become due; and (h) all financial information that Buyer has provided to MRP is true and accurate and fairly represents Buyer’s financial condition.

        12. PROPRIETARY RIGHTS.

(a) Ownership. No sale shall be construed as granting to Buyer any license or other right in, or to, any of MRP’s (i) patents; (ii) trademarks; (iii) internet domain names, whether or not trademarks, registered by any authorized private registrar or governmental authority, web addresses, web pages, websites and URLs; (iv) works of authorship, expressions, designs and design registrations, whether or not copyrightable, including copyrights and copyrightable works, software and firmware, technical data, data files, and databases and other specifications and documentation; (v) trade secrets; (vi) environmental or other testing applicable to the Equipment and/or the Services; and (vii) industrial and other intellectual property rights, and all rights, interests, and protections that are associated with, equivalent or similar to, or required for the exercise of, any of the foregoing, however arising, in each case whether registered or unregistered and including all registrations and applications for, and renewals or extensions of, such rights or forms of protection pursuant to the laws of any jurisdiction throughout in any part of the world (collectively, the “Intellectual Property Rights”).

(b) Prohibited Acts. Buyer shall not (i) take any action that might interfere with any of MRP’s rights in or to Intellectual Property Rights, including MRP’s ownership or exercise thereof; (ii) challenge any right, title, or interest of MRP in or to the Intellectual Property Rights; (iii) make any claim or take any action adverse to MRP’s ownership of the Intellectual Property Rights; (iv) register or apply for registrations, anywhere in the world, for MRP’s trademarks or any other trademark that is similar to MRP’s trademarks or that incorporates MRP’s trademarks in whole or in confusingly similar part; (v) use any mark, anywhere that is confusingly

similar to MRP’s trademarks in whole or in confusingly similar part; (vi) engage in any action that tends to disparage, dilute the value of or reflect negatively on the Equipment and/or the Services or any of MRP’s trademarks; (vii) misappropriate any of MRP’s trademarks for use as a domain name without prior written consent from MRP; or (viii) alter, obscure or remove any of MRP’s trademarks, or trademark or copyright notices or any other proprietary rights notices placed on the

Equipment, marketing materials or other materials that MRP may provide.

        13.  CONFIDENTIAL INFORMATION. Without the prior written consent of MRP,Buyer, directly or indirectly, shall not disclose (and will direct its directors, shareholders, employees and agents not to disclose) any Confidential Information. The term “Confidential Information” means any information of or relating to MRP or the Equipment and/or the Services not generally known to the public (other than as a result of disclosure in violation of this Agreement) in spoken, printed, electronic or any other form or medium, including, but not limited to, business processes, practices, methods, policies, plans, publications, documents, research, operations, services, strategies, techniques, agreements, contracts, transactions, potential transactions, know-how, trade secrets, databases, manuals, records, supplier information, financial information, accounting information, legal information, marketing information, pricing information, payroll information, personnel information, and supplier lists.

        14.  NON-SOLICITATION. Buyer agrees not to solicit or hire any personnel of MRP involved with the delivery of the Services during the provision of such Services and for twelve (12) months after the completion of such Services; provided, however, that Buyer may hire individuals employed by MRP who, without other solicitation, respond to advertisements or solicitations aimed at the general public.

        15.  EQUITABLE REMEDIES. Buyer acknowledges and agrees that (a) a breach or threatened breach by Buyer of any of its obligations under Sections 13 or 14 would give rise to irreparable harm to MRP for which monetary damages would not be an adequate remedy and (b) in the event of a breach or a threatened breach by Buyer of any such obligations, MRP shall, in addition to any and all other rights and remedies that may be available to MRP at law, at equity, or otherwise in respect of such breach, be entitled to equitable relief, including a temporary restraining order, an injunction, specific performance, and any other relief that may be available from a court of competent jurisdiction, without any requirement to post a bond or other security, and without any requirement to prove actual damages or that monetary damages will not afford an adequate remedy. Buyer agrees that Buyer will not oppose or otherwise challenge the appropriateness of equitable relief or the entry by a court of competent jurisdiction of an order granting equitable relief, in either case, consistent with the terms of this Section 15.

        16.  INDEMNIFICATION. Buyer agrees to indemnify, defend and hold harmless MRP and its directors, shareholders, employees and agents (collectively, “MRP Indemnitees”) against any liability, damage, loss or expense incurred by or imposed in connection with any claims, suits, actions, demands or judgments arising out of (a) any breach or non-fulfillment of any representation, warranty or covenant set forth in this Agreement by Buyer or its directors, managers, employees or agents (collectively, “Buyer’s Agents”); (b) any negligent act or omission or willful misconduct of Buyer or Buyer’s Agents in connection with this Agreement; (c) any bodily injury, death of any person or damage to real or tangible personal property caused by Buyer or Buyer’s Agents, including the use of unauthorized parts in or service of the Equipment; (d) any failure by Buyer or Buyer’s Agents to comply with any applicable laws; (e) any fraud or other intentional acts by Buyer or Buyer’s Agents; and (f) the use or operation of the Equipment, including, without limitation, any medical and/or surgical procedures performed by Buyer, and any of Buyer’s Agents, using the Equipment unless said damages are determined by a court of competence jurisdiction to be solely by the gross negligence of MRP or solely as result of a breach by MRP of the limited warranties contained herein.

        17.  DEFAULTS; REMEDIES. Notwithstanding anything herein to the contrary, should Buyer fail to pay for the order or any other amount, in whole or in part, when due or perform its other obligations under this Agreement or as otherwise mutually agreed in writing between Buyer and MRP (each, a “Default”), then MRP may take any and all actions available under law or equity to collect said amounts with a ten (10) day prior written notice, including, but not limited to, enforcing its security interest, accelerating the payment of and declaring immediately due and payable any unpaid balance of the order, referral to outside collection agencies and/or commencement of legal action. MRP’s rights shall be cumulative, and it shall not be required to have attempted to realize upon to the Equipment before taking any other collection actions. MRP may require that Buyer assemble and return any or all of the Equipment to MRP and, in the event Buyer fails to return such Equipment peaceably, enter upon the premises where such Equipment is located, with or without legal process, and repossess such Equipment. Upon a Default, Buyer agrees to pay upon MRP’s demand: (i) all costs and expenses incurred by MRP or its assignee in connection with the enforcement of any remedies, including all expenses incurred in connection with the return, sale, release or other disposition of the Equipment, including attorneys’ fees and other costs incurred by MRP or its assignee in enforcing or defending its rights and remedies under this Agreement and any other written agreement between Buyer and MRP.

        18.  COMPLIANCE WITH LAWS. Buyer shall (a) carry out the transactions contemplated by this sale and deal with the Equipment in conformity with all applicable laws, rules and regulations of all government authorities, including, without limitation, export laws, (b) obtain all permits and licenses required in connection with the purchase, shipment, installation or use of the Equipment, and (c) be solely responsible to fully understand and comply with laws, rules and regulations. Any information provided is as a convenience only.

        19.  FURTHER ASSURANCES. Upon MRP’s reasonable request, Buyer shall, at its sole cost and expense, execute and deliver all such further documents and instruments, and take all such further acts, necessary to give full effect to this Agreement.

        20.  ASSIGNMENT; SUCCESSORS AND ASSIGNS. Buyer cannot delegate any duties nor assign any rights or claims under this Agreement without MRP’s prior written consent, and any such attempt or assignment shall be void. In the event that Buyer finances its acquisition of any Equipment with a third party, Buyer may direct MRP to transfer title of such Equipment to such third-party financing company, with all remaining terms and conditions of this Agreement remaining in full force and effect. This Agreement is binding on and inures to the benefit of the parties to this Agreement and their respective permitted successors and permitted assigns.

        21.  NO THIRD-PARTY BENEFICIARIES. Subject to Section 16, this Agreement benefits solely the parties to this Agreement and their respective permitted successors and assigns, and nothing in this Agreement, express or implied, confers on any other person any legal or equitable right, benefit, or remedy of any nature whatsoever under or by reason of this Agreement.

        22.  GOVERNING LAW; VENUE. The application of the UN Convention on Contracts for the International Sale of Goods is expressly excluded. The parties agree that any and all claims, demands, disagreements, controversies or disputes arising out of or relating to this Agreement and any agreement or document delivered in connection herewith (collectively, “Claims”) shall be governed by and construed in accordance with the laws of the State of Utah and adjudicated exclusively in the state and federal courts located in or nearest to Summit County, Utah, which courts shall have the sole and exclusive jurisdiction and venue for adjudication of all Claims. The parties hereby agree upon, consent and stipulate to the jurisdiction and venue of the aforementioned courts for the adjudication of all Claims, to the exclusion of all other courts, forums and venues whatsoever.

        23.  NON-DISPARAGEMENT. Buyer shall not disparage MRP or MRP’s trademarks, websites, products or services, or display any such items in a derogatory or negative manner on any website or in any public forum or press release.

        24.  NOTICES. Any notice, demand, or communication required, permitted or desired to be given hereunder shall be deemed effectively given when personally delivered, when sent by electronic means, when received by overnight courier, or when mailed by prepaid, certified or registered mail, return receipt requested, addressed to the other party at its address set forth on the Quote or to such other address that the receiving party may designate from time to time in accordance with this Section 25.

        25.  PUBLIC ANNOUNCEMENTS. Unless otherwise stated herein, neither party shall issue a press release or otherwise advertise, make a public statement or disclose to any third-party information pertaining to the relationship arising under this Agreement, the existence or terms of this Agreement, the underlying transactions between MRP and Buyer or agent for Buyer or refer to the other party in relation to this Agreement without the other party’s prior written approval.

        26.  ENTIRE AGREEMENT; ADDITIONAL OR INCONSISTENT TERMS. Subject to Section 32, this Agreement constitutes the sole and entire agreement between the parties hereto relating to the subject matter hereof, and any unincorporated representation, affirmation of fact, course of prior dealings, promise or condition in connection therewith, or usage of the trade, shall not be binding on either party. Terms and conditions set forth which differ from, conflict with or are not included in this Agreement shall not be part of any agreement between MRP and Buyer unless both parties specifically accept such terms and conditions in writing.

        27.  WAIVER. No waiver under this Agreement is effective unless it is in writing and signed by the party waiving its right. Any waiver authorized on one occasion is effective only in that instance and only for the purpose stated and does not operate as a waiver on any future occasion. None of the following constitutes a waiver or estoppel of any right, remedy, power, privilege or condition arising from this Agreement: any failure or delay in exercising any right, remedy, power or privilege or in enforcing any condition under this Agreement; or any act, omission or course of dealing between the parties.

        28.  SURVIVAL. Subject to the limitations and other provisions of this Agreement, the representations and warranties of Buyer contained herein shall survive the expiration or earlier termination of this Agreement for a period of twelve (12) months after such expiration o termination and (b) this Section 29 and Sections 10, 12, 13, 14, 15, 16, 17, 21, 22, 23, 24, 26, and 32 of this Agreement, as well as any other provision that, in order to give proper effect to its intent, should survive such expiration or termination, shall survive the expiration or earlier termination of this Agreement. All other provisions of this Agreement shall not survive the expiration or earlier termination of this Agreement.

        29.  RELATIONSHIP OF PARTIES. Nothing in this Agreement creates any agency, joint venture, partnership or other form of joint enterprise, employment or fiduciary relationship between the parties. Neither party has any express or implied right or authority to assume or create any obligations on behalf of or in the name of the other party or to bind the other party to any contract, agreement or undertaking with any third party.

        30.  HEADINGS. The headings in this Agreement are for reference only and do not affect the interpretation of this Agreement.

        31.  ORDER OF PRECEDENCE. In the event of conflict between the Quote, a written agreement by MRP, and these Terms, the order of priority shall be: (1) the written

agreement by MRP, if only if executed by an MRP Officer, (2) the Quote and (3) these Terms, and only to the extent of the direct conflict. Notwithstanding the foregoing, MRP shall not be bound by, and specifically objects to, any terms, conditions or other provisions, both written and oral, which are different from, in addition to or inconsistent with the provisions of this Agreement which are set forth in any purchase order, receipt, acceptance, confirmation, correspondence or otherwise of, or by, Buyer. Fulfillment of Buyer’s order shall not constitute acceptance of any of Buyer’s terms and conditions and does not serve to modify or amend the terms and conditions contained herein.

        32.  SEVERABILITY. If any part of this Agreement is held to be void, illegal or unenforceable, then it shall be deemed to be severed from this Agreement and the remaining provisions shall continue in full force and effect; provided, however, that if any fundamental term or provision of this Agreement is held to be void, illegal or unenforceable, the remainder of this Agreement shall be unenforceable. Upon a determination that any term or provision is void, illegal or unenforceable, the parties shall negotiate in good faith to modify this Agreement to effect the original intent of the parties as closely as possible in order that the transactions contemplated hereby be consummated as originally contemplated to the greatest extent possible.