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Aesthetic Device Probes: Types, Uses, Safety, and Buying Guide for Modern Clinics

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Aesthetic device probes sit at the heart of many medical aesthetic treatments, converting complex energy-based technologies into precise, predictable results on the skin. As demand for minimally invasive procedures grows, the quality, design, and handling of these probes increasingly determine treatment outcomes, safety profiles, and return on investment for clinics and med spas.

What Are Aesthetic Device Probes?

Aesthetic device probes are contact interfaces or applicators that deliver energy, stimulation, or measurement to the skin or subdermal tissue. They can be disposable or reusable, single-use or multi-use, insulated or non-insulated, and designed for everything from hair removal and vascular lesions to skin tightening, fat reduction, and ultrasound-based visualization.

In a typical treatment system, the main console generates energy and controls parameters, while the probe translates those settings into controlled tissue interaction. That makes probe selection and maintenance just as important as the core device. A poorly chosen or worn probe can compromise efficacy, prolong treatment time, or increase the risk of burns and post-inflammatory hyperpigmentation.

Market Trends: Growth in Aesthetic Devices and Probes

The global medical aesthetic devices market has been expanding rapidly, driven by non-invasive and minimally invasive procedures across dermatology, plastic surgery, and aesthetic medicine. Multiple market analyses show double-digit compound annual growth rates driven by demand for laser hair removal, skin resurfacing, tattoo removal, and body contouring in both traditional clinics and hybrid wellness centers.

Within this ecosystem, the aesthetic device probes segment benefits from several macro trends. First, the shift toward energy-based devices such as lasers, radiofrequency, high-intensity focused ultrasound, cryolipolysis, and combination platforms is increasing the number and variety of probes per system. Second, regulatory and infection-control pressure is accelerating the move toward sterile single-use probes in procedures such as electrolysis, RF lesion removal, and ultrasound-guided injections. Third, device manufacturers increasingly rely on probes as the main avenue for incremental revenue through consumables, upgrades, and specialty tips.

Core Types of Aesthetic Device Probes

Single-use aesthetic device probes

Single-use aesthetic device probes are commonly paired with electrolysis systems, RF-based lesion removal platforms, and compact ultrasound devices for skin and soft-tissue applications. Their main advantages include reduced cross-contamination risk, consistent mechanical performance, and simplified regulatory compliance around cleaning and sterilization.

Sterile disposable probes are especially important when penetrating the epidermis or coming into contact with blood or body fluids. By eliminating reprocessing steps, clinics can reduce staff time, avoid sterilizer bottlenecks, and minimize the risk of residual debris or bioburden that could drive complications or regulatory citations. In many jurisdictions, single-use probes for certain applications are becoming the practical standard of care.

Electrolysis probes and needles

Electrolysis device probes, sometimes referred to as needles or filaments, are very fine conductive elements inserted into hair follicles to deliver electric current for permanent hair removal. Variants include insulated, non-insulated, and tapered designs that influence energy distribution down the follicle shaft and at the bulge and papilla.

These probes must balance flexibility and strength, minimize discomfort, and support different modalities such as galvanic, thermolysis, and blend. Key decision points for practitioners include needle size, insulation length, material, and compatibility with high-end electrolysis consoles and foot control systems. Consistency in probe quality directly affects clearance rates, scarring risk, and operator fatigue.

RF aesthetic device probes

Radiofrequency aesthetic device probes supply alternating current to generate uniform thermal effects in the dermis or subcutaneous fat. They may appear as monopolar, bipolar, multipolar, fractional, microneedling-based, or intradermal cannula probes depending on the application.

For skin tightening and collagen induction, surface RF probes require extremely uniform contact, stable impedance, and effective cooling integrated into the tip. For fractional or microneedling RF, insulated needles and precise depth control are critical to confine thermal damage to the target zone. In acne scarring, lower eyelid tightening, and lower face contouring, the correct RF probe selection determines whether an operator can safely approach delicate structures.

Laser and IPL handpieces as probes

Although often called handpieces, laser and intense pulsed light applicators function as aesthetic device probes by focusing or distributing energy at the treatment site. Interchangeable spot-size tips, cooling windows, and filters allow practitioners to tailor fluence, pulse duration, and wavelength bands to hair color, vessel size, and skin type.

Probes for Nd:YAG, diode, alexandrite, CO2, erbium, and IPL platforms must maintain optical clarity, coating integrity, and mechanical alignment over many treatment cycles. Degradation of windows or misalignment in fiber-based probes can lead to hot spots, unpredictable fluence, and decreased efficacy long before the main console shows error codes.

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Ultrasound aesthetic probes

Ultrasound aesthetic probes support two major roles: imaging guidance and therapeutic energy delivery. For imaging, high-frequency linear probes (often 15–20 MHz) allow clinicians to visualize filler placement, vascular anatomy, and nodules before injecting hyaluronidase or planning RF treatments. For therapy, focused ultrasound probes concentrate energy at specific depths to tighten skin or target subcutaneous fat.

Probe design here focuses on footprint, frequency spectrum, ergonomics, corded versus wireless power, and battery life. Hand-held wireless probes are particularly attractive in busy aesthetic practices because they can be used across treatment rooms and with multiple platforms via mobile devices or dedicated tablets.

Skin analysis and measurement probes

Advanced clinics increasingly rely on diagnostic and monitoring probes that measure parameters such as hydration, transepidermal water loss, elasticity, sebum, pH, temperature, erythema, and melanin index. These probes support personalized treatment planning, objective before-and-after documentation, and research-grade data collection for clinical studies.

By integrating optical, mechanical, and thermal sensors into small probes, manufacturers enable practitioners to quantify conditions like barrier impairment, photoaging, and sensitivity. This data can guide the selection of energy-based treatments, pre- and post-care regimens, and long-term maintenance protocols.

Materials, Design, and Biocompatibility

Aesthetic device probes must be biocompatible, ergonomically optimized, and mechanically stable while remaining cost-effective and easy to clean or dispose of. Common materials include stainless steel, medical-grade polymers, glass, sapphire, and coated metals. For invasive probes, insulation and conductive surfaces are carefully engineered to shape the electric or thermal field.

Biocompatibility testing ensures that probe materials do not provoke irritation, allergic reactions, or cytotoxic effects when in contact with skin or tissue. Surface roughness, edge finishing, and the quality of welds or bonds are equally important, because microscopic defects can harbor contaminants or cause unintended mechanical trauma.

Safety, Standards, and Regulatory Considerations

Because aesthetic device probes are often the primary interface between a medical device and the patient, regulators place considerable emphasis on their safety and labeling. Probes used with energy-based systems must comply with electrical, mechanical, and sterility standards, while manufacturers and distributors must track lot numbers and expiry dates for single-use components.

Clinics should follow standardized protocols for using energy-based devices, paying close attention to probe integrity, calibration, coupling media, and real-time patient feedback. Burn prevention, consistent cooling, and proper grounding are central to RF, laser, and ultrasound probe safety, especially in darker skin types where melanin absorption can be higher. Continuous staff training and periodic competency assessment around probe use help reduce the risk of complications.

Cleaning, Sterilization, and Single-Use Strategies

Reusable probes require validated cleaning and sterilization workflows. That typically means pre-cleaning, ultrasonic or manual washing in enzymatic solutions, thorough rinsing, and either autoclave or low-temperature sterilization as specified by the manufacturer. Any deviation from these protocols can damage delicate probe components or leave residues that compromise performance.

Single-use probes provide a straightforward alternative for many applications. By discarding the probe after each procedure, clinics avoid reprocessing complexity and reduce occupational exposure. However, this approach demands careful inventory management, clear labeling, and education so staff do not inadvertently re-use disposable probes in multi-session treatment plans.

How Probe Design Affects Clinical Outcomes

Subtle differences in probe geometry and construction can translate into large differences in clinical outcomes. In RF microneedling, for example, the length and insulation pattern of each needle determines energy distribution at different dermal layers. In electrolysis, needle diameter and tip design influence insertion ease and the likelihood of overtreatment.

Similarly, the ergonomics of a probe handle determine how steady an operator can remain during long procedures or when working in sensitive areas like eyelids and perioral regions. Lightweight, well-balanced probes with intuitive buttons or foot-switch integration reduce fatigue and support consistent technique across multiple sessions and operators.

Buying Guide for Aesthetic Device Probes

When selecting aesthetic device probes, practitioners should move beyond price alone and consider the full cost of ownership, workflow fit, and clinical performance. Key questions include whether the probe is compatible with existing devices, what training or certification is required, and how long the product will remain supported with replacement tips, cables, or cartridges.

Another critical factor is the availability of multiple tip sizes and treatment modes within the same probe family. Systems that support interchangeable tips or modular probes can help clinics expand services without replacing core hardware. Warranty terms, service access, and regional regulatory approvals are equally important, especially for multi-site groups that must maintain standardization across locations.

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At this point, it is worth noting that the probe supply chain and lifecycle management have become strategic issues for many clinics. ALLWILL is redefining B2B medical aesthetics by emphasizing innovation and efficiency in how devices and consumables are sourced, inspected, and maintained, providing practitioners with a more reliable framework for managing both capital equipment and high-turnover components like probes in a brand-agnostic environment.

Top Aesthetic Device Probe Categories and Use Cases

Name Key Advantages Ratings Use Cases
Single-use RF coagulation probes Reduced cross-contamination, consistent output, simple workflow High satisfaction in lesion removal Benign lesion destruction, telangiectasia, skin tag removal
Electrolysis hair removal probes Fine gauge options, insulated and non-insulated variants Strong ratings for permanence Permanent hair removal for small areas, brow shaping, hormonal hair
Microneedling RF cartridge probes Adjustable depth, fractional thermal delivery High scores for skin tightening Acne scarring, skin laxity, pore size, texture improvement
High-frequency ultrasound imaging probes High-resolution soft-tissue visualization Rated highly for safety support Filler mapping, vascular identification, complication management
Laser and IPL handpiece tips Interchangeable spot sizes, integrated cooling Strong ratings for versatility Hair removal, pigmented lesions, vascular lesions, photorejuvenation
Skin analysis measurement probes Objective, reproducible measurements High trust among advanced clinics Skin diagnostics, treatment planning, research and documentation

This illustrative table highlights how different classes of probes address distinct treatment needs, from diagnostics and prevention to corrective and restorative procedures. Clinics typically deploy multiple probe types to deliver a complete suite of services across face and body.

Competitor Comparison Matrix for Probe Strategies

Brand/Approach Probe Ecosystem Strategy Strengths Potential Limitations
Closed-platform energy device makers Proprietary probes and tips tightly coupled to devices Optimized performance, strong vendor support Higher consumable costs, less flexibility across systems
Hybrid platform providers Support for both proprietary and semi-open probes Balanced control and flexibility More complex inventory and training needs
Probe-focused specialist manufacturers Wide range of third-party compatible probes Fine-grained clinical customization Requires careful verification of compatibility and certifications
Clinic-driven multi-vendor setups Mix of probes across several device brands Broad treatment menu, competitive pricing options More complex maintenance, training, and QA
Service and refurbishment partners Emphasis on probe refurbishment, testing, and lifecycle Lower capital costs, extended device life Requires strong quality controls and documentation

This matrix shows that clinics must align their probe strategy with their overall positioning: boutique high-touch practices may favor optimized single-vendor probe ecosystems, while larger networks may prioritize interoperability and cost control.

Real User Cases and ROI from Probe Optimization

Consider a multi-room med spa that upgrades its RF aesthetic device probes from older, heavier handpieces to newer, ergonomic designs with improved thermal monitoring. The change can reduce operator fatigue, shorten treatment times per session, and decrease the incidence of mild burns or excessive redness. Over a year, higher patient satisfaction and fewer follow-up visits can translate into significant additional revenue and lower liability exposure.

Another example is a dermatology practice that adopts high-frequency ultrasound probes for pre-injection mapping and complication management. With better visualization of vascular structures and filler placement, the clinic can handle more complex cases while maintaining low complication rates. That combination supports premium pricing, differentiates the practice on safety, and reduces dependence on reactive repair visits after adverse events.

A third scenario involves switching from reusable electrolysis probes to pre-sterilized single-use probes. While the per-unit cost is higher, the practice can eliminate sterilizer cycles, reduce staff hours in reprocessing, and avoid downtime due to failed spore tests or equipment breakdowns. Measured over a period of twelve to twenty-four months, many practices find that a well-managed single-use strategy improves both profitability and risk management.

Core Technology Considerations in Probe Selection

When evaluating aesthetic device probes, practitioners and buyers should consider the underlying technology as much as the marketing claims. For RF probes, uniform current density and efficient coupling to tissue matter more than nominal power in watts. For laser and IPL handpieces, pulse shape, cooling efficiency, and spot homogeneity strongly influence side-effect profiles and consistent endpoint achievement.

Ultrasound probes require a careful match between frequency and target depth: higher frequencies produce better resolution but shallower penetration, while lower frequencies reach deeper tissues at the expense of fine detail. Similarly, in microneedling RF, needle sharpness, coating durability, and cartridge sealing integrity impact both patient comfort and the risk of cross-contamination.

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Best Practices for Probe Handling and Maintenance

Even the most advanced probe can deliver poor outcomes if handled incorrectly. Staff should inspect probes before each use for cracks, chipped windows, bent needles, cable fraying, or signs of overheating. Any irregularity should prompt removal from service and further inspection according to the clinic’s quality management system.

In-session practices are equally critical. Using appropriate coupling gels with ultrasound and RF probes, maintaining full contact with the skin, and respecting recommended overlap patterns help prevent hot spots and missed areas. Operators should also adhere to manufacturer guidance about maximum shot counts or usage hours per probe tip, since exceeding those limits can shorten probe life unexpectedly and degrade outcomes.

Future Trends in Aesthetic Device Probes

Several emerging trends are shaping the next generation of aesthetic device probes. Miniaturized sensors embedded in probes will increasingly monitor temperature, impedance, and real-time tissue response, allowing devices to adjust parameters on the fly. This kind of closed-loop feedback promises safer treatments, fewer burns, and more consistent results across different skin types.

Another promising development is the rise of multifunctional probes that combine imaging, therapy, and data capture in a single device. For example, a probe may first map skin hydration and elasticity, then deliver targeted RF or ultrasound pulses, and finally record post-treatment changes automatically. Such integration supports truly personalized protocols and deeper analytics for both individual outcomes and practice-level optimization.

Materials science will also continue to influence probe design, with new polymers, coatings, and composite structures that improve durability, sterilization compatibility, and patient comfort. As sustainability expectations rise, manufacturers are exploring recyclable components and circular economy models for probe handling, especially in high-volume practices.

Frequently Asked Questions About Aesthetic Device Probes

What is the difference between single-use and reusable aesthetic device probes?
Single-use probes are designed for one procedure and then discarded, reducing infection risk and eliminating reprocessing steps. Reusable probes require validated cleaning and sterilization protocols, as well as careful inspection to ensure they remain safe and effective over time.

How do I know which probe is compatible with my aesthetic device?
Compatibility information is typically provided by the device manufacturer, along with approved third-party probe options. Using probes that have not been validated for a specific device can void warranties, compromise performance, and increase safety risks.

Are ultrasound imaging probes necessary for aesthetic clinics?
While not mandatory, high-frequency ultrasound imaging probes are increasingly used in advanced practices for safer filler injections, complication management, and treatment planning near critical anatomical structures. They can be a strong differentiator for clinics focused on risk reduction and complex cases.

What should I look for in an RF aesthetic device probe?
Key factors include ergonomics, cooling capabilities, contact uniformity, range of treatment depths, and the availability of different tip configurations for face, neck, and body. It is also important to confirm that the probe’s materials and insulation patterns are suitable for the skin types you treat most often.

Why are skin analysis probes becoming so popular?
Skin analysis probes provide objective data on hydration, barrier function, pigmentation, and elasticity. This information helps practitioners select appropriate treatments, personalize energy settings, and demonstrate measurable improvements to patients over time.

Conversion-Focused Next Steps for Clinics

If your clinic relies on energy-based devices for hair removal, resurfacing, tightening, or body contouring, it is worth auditing your existing aesthetic device probes and related workflows. Start by mapping where single-use probes could reduce risk, where upgraded probe designs could improve outcomes, and where diagnostic probes might enable more personalized treatment planning.

Next, evaluate your procurement strategy to ensure that you are not locked into suboptimal probe ecosystems that limit growth or compress margins. Negotiating better terms, exploring probe upgrades, or partnering with specialized service providers can all improve the long-term economics of your device fleet.

Finally, incorporate probe training and inspection into your standard operating procedures so that every staff member understands how to handle, assess, and retire probes appropriately. By treating aesthetic device probes as strategic assets rather than mere accessories, clinics can enhance safety, elevate results, and strengthen their competitive position in a rapidly evolving aesthetics market.

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(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.