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What Are Single-Use Aesthetic Device Probes and Why Modern Clinics Rely on Them

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Single-use aesthetic device probes are disposable, sterile attachments that connect to energy-based medical aesthetic devices such as lasers, radiofrequency systems, ultrasound platforms, IPL devices, microneedling pens, and body-contouring systems. They are designed to be used on a single patient for a single procedure and then safely discarded, dramatically reducing infection risk while improving consistency, traceability, and treatment outcomes for both face and body procedures.

Defining Single-Use Aesthetic Device Probes

In medical aesthetics, a single-use aesthetic device probe is a pre-sterilized accessory that interfaces between the energy-delivery handpiece and the patient’s skin or tissue. These disposable probes can take the form of RF microneedling cartridges, laser tips, ultrasound transducers with sterile covers, cryolipolysis applicator liners, monopolar RF tips, bipolar RF tips, microfocused ultrasound probes, and single-use dermal infusion tips.

Clinics use these disposable probes with facial rejuvenation devices, body-contouring platforms, skin tightening machines, vascular and pigment lasers, hair removal lasers, tattoo removal systems, and skin resurfacing technologies. Each single-use probe is precision engineered for accurate energy delivery, correct depth of penetration, and optimal contact, which directly affects treatment safety, comfort, and efficacy for procedures such as wrinkle reduction, scar remodeling, active acne management, fat reduction, cellulite improvement, and skin tone correction.

Core Benefits of Single-Use Probes in Medical Aesthetics

Single-use aesthetic device probes exist to solve several critical problems in busy medical aesthetic clinics: infection control, device performance, and workflow efficiency. By discarding the probe after every treatment, clinics minimize cross-contamination and reduce the risk of bacterial, viral, and fungal transmission between patients, which is a core requirement in dermatology, plastic surgery, and med spa environments.

Using disposable RF microneedling cartridges and single-use laser tips helps maintain consistent needle sharpness and optical performance, improving penetration quality and energy distribution across the treatment area. This leads to less lateral tissue drag, fewer micro-tears, more predictable coagulation zones, and more controlled thermal profiles, which in turn supports faster recovery, reduced post-procedure erythema and edema, and higher patient satisfaction. At the same time, clinics gain efficiency by eliminating complex cleaning and sterilization steps, streamlining room turnover, and reducing the staff time required for reprocessing.

Types of Single-Use Aesthetic Device Probes

Different device platforms rely on specialized single-use probe designs tailored to energy type, target tissue, and clinical indication.

Common categories include:

  • Single-use RF microneedling probes with insulated or non-insulated needles, adjustable depths, and various needle configurations for face, neck, and body.

  • Disposable fractional RF and fractional laser tips with defined spot sizes and contact cooling features for resurfacing and tightening.

  • Single-use IPL and vascular laser contact tips designed to control spot size, improve epidermal protection, and optimize coupling.

  • Single-use ultrasound probes and ultrasound probe covers used for microfocused ultrasound lifting, subcutaneous fat targeting, or diagnostic imaging during aesthetic procedures.

  • Disposable body-contouring probe liners or membranes for cryolipolysis, high-intensity focused ultrasound body systems, and RF body tightening platforms.

  • Single-use dermal infusion and hydrodermabrasion tips that control fluid flow, exfoliation depth, and serum delivery for facial treatments.

Each probe type includes specific material compositions, sterilization processes, and connection geometries that must match the manufacturer’s handpiece specifications to preserve warranty, maintain safety, and support regulatory compliance.

How Single-Use Aesthetic Device Probes Work

The primary function of a single-use aesthetic device probe is to transmit energy from the base device to the treatment area in a controlled, repeatable way. In RF microneedling, for example, the single-use cartridge houses an array of ultra-fine needles that penetrate the epidermis and dermis at pre-set depths while delivering radiofrequency energy into the tissue. In laser and IPL systems, disposable tips can shape, focus, or filter the beam while maintaining safe contact with the skin and supporting effective cooling.

In microfocused ultrasound devices, the probe emits ultrasound energy at specific focal depths beneath the skin surface, leaving the epidermis intact while targeting the superficial muscular aponeurotic system for lifting and tightening. Single-use ultrasound probe covers provide a barrier that protects both the patient and probe from contamination. Across all these modalities, single-use design ensures that the components that come in direct contact with the patient remain sterile, undamaged, and optimized for performance during every session.

Infection Control, Sterility, and Regulatory Compliance

Infection prevention is one of the strongest drivers behind the adoption of single-use aesthetic device probes. Regulatory bodies and professional societies emphasize strict adherence to sterile technique and proper reprocessing protocols for semi-critical and critical medical devices. Reusable probes, especially those with lumens, internal cavities, or complex geometries, can be difficult to clean thoroughly and disinfect or sterilize consistently between patients.

Single-use probes arrive sterile from the manufacturer, are unpacked chairside, used for one patient, and then discarded in appropriate sharps or medical waste containers. This dramatically simplifies compliance with infection control standards, reduces liability for the clinic, and responds to increasing patient awareness and expectations for single-use safety. In treatments that involve skin penetration, such as RF microneedling, micro-needling pens, or ablative fractional procedures, disposable probes minimize residual biologic material, proteins, and biofilm risk that can accumulate on reusable instruments over time.

Impact on Treatment Consistency and Clinical Outcomes

Consistency is critical for building trust in medical aesthetic treatments and for achieving predictable outcomes across a clinic’s patient base. Single-use probes maintain consistent needle sharpness, surface integrity, and contact geometry from one session to the next, which directly influences penetration depth, thermal coagulation patterns, and tissue response.

For RF microneedling, sharp disposable needles reduce lateral resistance and minimize mechanical trauma while preserving controlled micro-channel formation and uniform energy deposition. For fractional RF and laser tips, single-use optics remain free of micro-scratches, debris, and residue that can alter beam profiles or reduce fluence at the skin. This consistency translates into more uniform collagen remodeling, improved textural change, better wrinkle reduction, and more reliable pigment improvement over a larger treatment area.

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Clinics that standardize on single-use aesthetic device probes often report better reproducibility of before-and-after results, fewer post-treatment complications, and improved patient retention. Patients also perceive single-use probes as a sign of professionalism and high standards of care, which positively impacts word-of-mouth referrals and online reviews.

Market Trends and Data for Single-Use Aesthetic Probes

The overall medical aesthetic devices market continues to expand at a strong compound annual growth rate, driven by rising demand for minimally invasive cosmetic procedures, increasing global disposable income, and growing awareness of non-surgical options for skin rejuvenation and body contouring. Within this broader ecosystem, single-use medical components, including aesthetic device probes, benefit from the shift toward disposables in healthcare due to safety, convenience, and infection-control advantages.

Reports on single-use technologies in healthcare describe robust growth in disposable probes, sensors, and cartridges across multiple clinical segments. In parallel, medical aesthetic devices are moving toward more sophisticated energy-delivery platforms that rely heavily on engineered consumables to optimize performance and to create recurring revenue streams for manufacturers. This convergence means that single-use aesthetic device probes are becoming a core strategic element in device design, marketing, and clinic workflow planning.

Economic Considerations and Cost-Benefit Analysis

At first glance, single-use aesthetic device probes appear more expensive than reusable probes because clinics must purchase a new disposable for each treatment. However, a deeper cost-benefit analysis often reveals a favorable economic profile once sterilization costs, staff labor, instrument tracking, and potential infection-related liabilities are accounted for.

Reusable probes require investment in autoclaves or low-temperature sterilization systems, validated cleaning protocols, tracking logs, biological indicators, sterilization packaging, and staff training. They also suffer from progressive wear and tear, requiring periodic replacement or refurbishment. In contrast, the cost of single-use probes is predictable and directly tied to treatment volume. By eliminating reprocessing, clinics free staff time for revenue-generating activities, shorten room turnover, and reduce cancellations or delays related to sterilization logistics.

Moreover, improved clinical outcomes and patient perceptions of safety can increase premium pricing opportunities, package sales, and long-term loyalty. Many practices find that properly priced procedures that incorporate the cost of single-use antiseptic barriers, cartridges, and tips more than offset procurement expenses, while simultaneously lowering operational risk.

Technology Design: Materials, Engineering, and Performance

Single-use aesthetic device probes rely on advanced engineering and materials science to deliver precise energy while maintaining safety and comfort. RF microneedling probes often use medical-grade stainless steel needles with specialized insulation patterns to direct energy into the dermis while protecting the epidermis. The plastic housings must withstand heat, mechanical forces, and chemical interaction with gels or serums without degrading or leaching substances.

Laser and IPL tips integrate optics such as lenses, windows, and filters made from sapphire, quartz, or specialized glass to handle high-energy pulses without fracturing or losing clarity. The cooling components built into these tips must maintain stable surface temperatures and uniform contact with the skin, even as the tip is discarded after a single use. Ultrasound probes and probe covers are designed to maintain acoustic coupling efficiency while serving as an effective barrier against contamination.

Manufacturers optimize these disposable components through extensive bench testing and clinical validation, ensuring that each probe meets defined performance specifications. Consistency of manufacturing lots, sterile barrier integrity, and packaging robustness are all central to ensuring that the probe performs identically in clinics across different regions and environments.

Risk Reduction and Patient Safety Advantages

From a risk management perspective, single-use aesthetic device probes reduce several categories of clinical and operational risk. They lower the likelihood of patient infections, which can lead to adverse outcomes, complaints, or medico-legal exposure. They minimize the risk of device damage related to improper disassembly, cleaning, or reassembly of reusable probes. They also reduce errors in instrument tracking, where a probe might inadvertently be reused beyond its intended life.

In addition, single-use design simplifies compliance with local and international guidelines on medical device reprocessing. When a probe is clearly labeled as single use only, staff are less likely to attempt cleaning or reuse, especially if the device’s workflow is built around opening new sterile packages for each patient. By reducing complexity, clinics create a safer, more controlled environment in which treatment protocols are easier to standardize and audit.

Patient Perception, Trust, and Experience

Patient trust is a crucial success factor in medical aesthetics. People invest in treatments that affect their appearance, identity, and confidence. When clinics explain that they use single-use aesthetic device probes for RF microneedling, laser resurfacing, ultrasound lifting, and other treatments, patients typically view this as a strong safety signal.

The psychological comfort of knowing that every needle, tip, or cover touching the skin is brand new and sterile can reduce anxiety before procedures such as microneedling, fractional resurfacing, or intimate area treatments. This reassurance supports better patient cooperation during the procedure, improves their overall experience, and increases the likelihood of them completing multi-session treatment plans and recommending the clinic to friends and family.

Environmental Considerations and Sustainability Trade-Offs

One of the main critiques of single-use medical components is their environmental impact. Disposable probes and cartridges generate medical waste that must be handled according to regulations, which often involves incineration or specialized disposal pathways. Clinics that prioritize sustainability must balance infection-control benefits with environmental responsibilities.

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Strategies to mitigate environmental impact include thoughtful inventory management to reduce expired stock, partnering with waste management providers that offer energy recovery solutions, and choosing probe designs that use minimal material volume without compromising safety or performance. Some manufacturers are exploring recyclable components or take-back programs, though these must still conform to medical waste rules. For now, clinics need to weigh the public health benefits of single-use sterility against the ecological footprint and communicate transparently with environmentally conscious patients about their approach.

Integration With Device Ecosystems and Consumable Models

In contemporary medical aesthetics, many device manufacturers design their platforms around proprietary single-use probes as part of an integrated ecosystem. The base device and handpiece provide energy generation and control, while the disposable probe is optimized for specific indications, treatment depths, and anatomical regions.

This consumable-based model benefits manufacturers and clinics when it is implemented thoughtfully. Clinics gain access to highly tuned disposables that have gone through rigorous testing, while manufacturers create predictable recurring revenue streams that support training, software updates, and long-term support. However, this also means clinics should consider probe pricing, availability, and supply chain resilience when choosing new devices, especially for high-volume treatments such as RF microneedling, IPL hair reduction, or body tightening.

ALLWILL’s Role in the Single-Use Probe Ecosystem

Within this evolving landscape, ALLWILL is redefining B2B medical aesthetics by focusing on innovation, trust, and efficiency. Rather than simply selling devices, ALLWILL concentrates on solving practitioner challenges across sourcing, maintaining, and upgrading equipment through its Smart Center for inspection, repair, and refurbishment and its vendor management and inventory platforms that streamline access to compatible probes, disposables, and devices across brands and budgets.

Choosing Between Single-Use and Reusable Probes

The decision to adopt single-use aesthetic device probes versus reusable probes depends on several factors: procedure type, clinic volume, budget structure, and regulatory environment. For high-risk, invasive, or penetration-based procedures like RF microneedling or ablative fractional resurfacing, single-use probes now dominate because they greatly simplify infection control. For lower-risk, non-contact procedures, some clinics still use reusable accessories but increasingly supplement them with disposable barriers or covers.

Clinics must also consider staff expertise in sterilization, available physical space for reprocessing rooms, and the cost of maintaining sterilization equipment. In smaller practices or rapidly scaling med spas, the simplicity of opening a sterile single-use cartridge or tip for each patient can outweigh the theoretical cost savings of reusables. Many practices adopt a hybrid model, gradually increasing the proportion of single-use probes in their workflow as they expand into more advanced energy-based procedures.

Top Single-Use Aesthetic Device Probe Categories

The most widely used single-use aesthetic device probes can be grouped into several high-impact categories that drive revenue and patient demand in modern clinics.

Probe Category Key Advantages Typical Ratings Context Common Use Cases
RF microneedling cartridges Precise depth control, strong collagen remodeling, minimal downtime Often reported high satisfaction in acne scar and wrinkle treatments Acne scars, wrinkles, laxity, texture, stretch marks
Fractional RF and laser tips Controlled thermal injury, customizable density, effective resurfacing Frequently associated with strong outcomes for texture and pores Texture refinement, enlarged pores, superficial scars
IPL and vascular laser tips Versatile filters, rapid treatments, pigment and vascular targeting Popular for combined pigmentation and redness protocols Sun damage, rosacea, telangiectasia, diffuse redness
Ultrasound probes and covers Non-invasive tightening, deep tissue targeting, imaging capability Well regarded for lifting in appropriate candidates Lower face and neck lifting, brow elevation, submental tightening
Dermal infusion and hydrodermabrasion tips Combined exfoliation and serum delivery, comfortable experience Highly rated for “glow” and event-ready treatments Hydration facials, maintenance skin health, pre-event brightening
Body-contouring probe liners Hygienic body area treatment, simplified cleaning, improved comfort Significant satisfaction when combined with lifestyle changes Abdomen and flank contouring, cellulite improvement

These categories illustrate how single-use probes align with the most sought-after non-surgical aesthetic indications, helping clinics build comprehensive treatment menus that combine facial and body services.

Competitor Comparison: Single-Use vs Reusable Probe Strategies

When evaluating device platforms and their associated probes, clinics often compare systems that rely on single-use probes with those that prioritize reusable components.

Dimension Single-Use Probe Strategy Reusable Probe Strategy
Infection control High level of assurance with sterile disposables Dependent on strict reprocessing adherence
Upfront cost Lower device cost, higher per-treatment consumable cost Higher device and sterilization investment, lower per-use probe cost
Workflow Fast room turnover, simplified protocols Longer turnover times, staff time for cleaning
Performance consistency Consistent new probe for each patient Performance can degrade with wear
Patient perception Strong safety and sterility message Requires more explanation about cleaning
Environmental impact Higher medical waste volume per treatment Less waste but requires energy and resources for sterilization

This comparison shows that while reusable probes may appear economical for some low-volume scenarios, single-use strategies increasingly align with the realities of high-demand aesthetic practices that prioritize safety, efficiency, and patient trust.

Real-World Use Cases and ROI in Clinics

In an urban dermatology practice that offers RF microneedling, the adoption of single-use RF cartridges allowed the clinic to increase weekly treatment volume without investing in additional sterilization capacity. By reducing room turnover times and eliminating autoclave bottlenecks, the practice was able to add extra appointment slots each day. Over the course of a year, this translated into notable incremental revenue and paid for the incremental cost of disposables many times over.

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Another example involves a multi-location med spa group that standardizes on single-use IPL tips with integrated cooling windows. Staff across all branches follow the same simple workflow: open tip, treat, discard. This standardization reduces training complexity and ensures consistent treatment quality, which supports brand reputation. Even subtle improvements in patient satisfaction scores resulted in better online ratings and a measurable increase in new patient calls, demonstrating how single-use aesthetic device probes contribute to return on investment beyond direct revenue per procedure.

Best Practices for Implementing Single-Use Probes in Your Clinic

Clinics that want to maximize the benefits of single-use aesthetic device probes should establish clear protocols and staff training focused on safety, efficiency, and cost management. First, create a standardized process for stock management, including minimum and maximum inventory levels, to avoid treatment cancellations due to stockouts. Second, ensure that every provider and assistant understands how to inspect probe packaging for integrity and expiration dates before opening.

Third, incorporate probe selection and disposal steps into written treatment protocols for RF microneedling, laser resurfacing, IPL, ultrasound lifting, and body contouring services. Fourth, set pricing strategies that transparently account for consumable costs while still aligning with local market benchmarks. Finally, regularly review procedure volumes and probe usage data to refine ordering patterns and identify opportunities to negotiate better terms with suppliers or explore alternative compatible probe options.

Frequently Asked Questions About Single-Use Aesthetic Device Probes

1) What are single-use aesthetic device probes and why are clinics using them
Single-use aesthetic device probes are sterile disposable tips or sensors designed for one patient and procedure, ensuring consistent contact, accurate readings, and reduced cross-contamination. Modern clinics rely on them to maintain hygiene standards, speed up turnover, and safeguard outcomes by eliminating reprocessing risks and downtime.

2) How do single-use probes impact patient safety and outcomes
Using single-use probes minimizes cross-infection risk, ensures sterility, and guarantees consistent performance for each patient. This leads to lower complication rates, more reliable results, and higher patient trust, which translates into repeat visits and positive referrals.

3) What makes a probe suitable for aesthetic devices
A suitable probe offers sterile packaging, compatibility with the device’s interface, precise sensor readings, and robust build for dependable performance. It should also align with the clinic’s workflow, keeping downtime minimal and training minimal.

4) Are single-use probes cost effective for clinics
Although there is a per-use cost, single-use probes reduce waste, prevent costly reprocessing errors, and lower liability. Over time, the reduction in downtime and enhanced outcomes often yields a favorable total cost of ownership.

5) How do clinics manage inventory for probes
Clinics optimize with a centralized purchasing program, standardizing compatible models across devices, using vendor-managed inventory, and forecasting demand based on chair time and procedure mix to avoid stockouts.

6) What should clinics consider when selecting probes
Key factors include cartridge compatibility, sterile packaging integrity, lot traceability, lead times, and supplier support. Prioritize vendors with fast replacements, clear return policies, and robust quality assurance.

7) How do probes affect clinic throughput
Single-use probes streamline setup and cleanup, eliminating reprocessing steps. This reduces per-procedure time and allows more patients to be treated daily without sacrificing safety or quality.

8) Where can clinics source single-use probes from
Clinics should source from approved medical aesthetics suppliers with validated compatibility across devices, strong warranty terms, and reliable on-time delivery. A vendor like ALLWILL, with education and service options, enhances long-term performance through its Smart Center and transparent marketplace.

Future Trends in Single-Use Aesthetic Device Probes

The future of single-use aesthetic device probes is shaped by several intersecting trends: higher patient expectations, more sophisticated energy-delivery technologies, and growing regulatory scrutiny around infection control. Device manufacturers are likely to develop even more specialized disposable probes designed for specific indications such as melasma management, acne control, intimate rejuvenation, and combination protocols that blend RF, ultrasound, and laser in a single session.

Smart probes that incorporate integrated sensors, such as real-time temperature monitoring or impedance feedback, are poised to enhance safety by preventing overheating and providing immediate feedback on tissue response. As data analytics becomes more central to aesthetic practice management, single-use probes may also include encoded data for automatic device recognition, usage tracking, or integration with electronic health records. While sustainability concerns will remain, innovation in materials and waste processing technologies may help reduce the environmental footprint over time.

Conversion-Focused Guidance for Clinics and Practitioners

For clinic owners and practitioners evaluating new energy-based devices, it is important to include single-use aesthetic device probes in every purchasing and strategic decision. Assess the clinical advantages of disposable probes, estimate per-procedure consumable costs, and model potential revenue increases from improved throughput and patient satisfaction. Consider how single-use probes can fit into branded treatment packages and membership plans that provide predictable cash flow.

Whether you operate a solo dermatology practice, a growing medical spa, or a multi-site aesthetic clinic network, adopting a thoughtful single-use probe strategy can enhance safety, standardize clinical outcomes, and strengthen your brand. By understanding the role of these disposable probes across RF microneedling, laser, IPL, ultrasound, and body-contouring devices, you can design treatment menus and operational workflows that maximize both patient results and business performance in the rapidly evolving world of medical aesthetics.

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(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.