HANDPIECES

Which Handpieces Work with Advanced Aesthetic Devices for Safe, Effective Treatments?

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Understanding which handpieces work with advanced aesthetic devices is critical for safety, clinical outcomes, and long-term return on investment. The right device–handpiece pairing directly affects treatment efficacy, patient comfort, and the scalability of your service menu.

Why Handpiece Compatibility Matters in Advanced Aesthetic Devices

Handpieces are not generic accessories; they are engineered around specific energy platforms such as diode lasers, Nd:YAG lasers, IPL, RF microneedling, HIFU, and CO₂ or Er:YAG resurfacing systems. Each platform has its own power requirements, cooling strategy, wavelength, and pulse architecture, which means not every handpiece can or should be connected to every base unit.

Manufacturers design advanced aesthetic platforms with proprietary connectors, calibration profiles, and safety interlocks. This ensures that energy delivery, pulse duration, contact cooling, and spot size match what the software is expecting for a given handpiece, minimizing the risk of burns, under-treatment, or device damage.

Core Types of Handpieces Used in Aesthetic Platforms

Most modern aesthetic systems rely on a relatively standard set of handpiece archetypes, tailored to specific treatment indications and body zones. Laser hair removal platforms commonly use diode handpieces with fixed or interchangeable spot sizes and integrated cooling to target melanin in the follicle while protecting the epidermis.

CO₂, Er:YAG, and other resurfacing platforms use fully ablative or fractional handpieces that modulate energy density, scan patterns, and treatment depth. These can shift between aggressive resurfacing for deep wrinkles and gentler fractional modes for texture, scars, and pigmentation while remaining compatible with the same laser engine.

Handpieces for Laser Hair Removal Devices

Diode laser hair removal devices typically pair with handpieces optimized around a single or blended wavelength such as 755 nm, 808 nm, or 810–1064 nm. These handpieces include sapphire or glass tips and active cooling technologies to increase fluence tolerance and reduce pain while maintaining efficient energy delivery into the follicle.

Some multi-wavelength systems allow the same handpiece to alternate or mix Alexandrite and Nd:YAG energy, giving clinics flexibility to treat lighter and darker phototypes without swapping the entire device. The key compatibility concern here is ensuring that the base unit’s power supply and software are calibrated for the specific diode stack and cooling hardware in the handpiece.

Handpieces for Fractional and Ablative Resurfacing Lasers

Advanced fractional lasers and CO₂ platforms often support multiple resurfacing handpieces that adjust beam profile, scan speed, and microthermal zone density. A single CO₂ engine may drive a more aggressive ablative scanner for deep resurfacing and a gentler fractional or hybrid tip for fine lines, pigment, and texture issues.

Er:YAG and hybrid fractional systems use handpieces that carefully shape the energy column to balance ablation and coagulation. Compatibility is tightly tied to how the scanner motor, optics, and fiber delivery line up with the laser source, so cross-system mixing of resurfacing handpieces is typically not recommended without explicit manufacturer approval.

Handpieces for IPL and Vascular Treatment Devices

Intense Pulsed Light platforms usually employ interchangeable filter-based handpieces, each tuned for hair removal, pigmentation, acne, or vascular lesions. These IPL handpieces share a common xenon flashlamp engine but use different wavelength cut-off filters and cooling designs, which is why compatibility is often limited to specific system series and generations.

For vascular and leg vein work, Nd:YAG or KTP laser handpieces with smaller spot sizes and high peak powers are common. A single aesthetic platform can offer both IPL and vascular laser handpieces, but their connectors, calibration chips, and internal cooling paths must match what the device firmware expects.

RF Microneedling Handpieces and Platform Compatibility

Modern RF microneedling platforms rely on dedicated handpieces that control needle depth, RF power, and pulse duration across different body zones. A typical RF system may include superficial face handpieces, deeper body handpieces with additional cooling, and precision tips for periocular or perioral work, all driven by the same RF generator.

Also check:  Clinical-Grade Handpieces in Medical Aesthetic Treatments: Definition, Safety, and Future Trends

These handpieces vary by needle count, insulation pattern, and penetration depth range. Compatibility is managed via chip recognition and software presets to ensure that face-specific tips are not used at unsafe energy levels on thin skin or delicate zones. Attempting to adapt RF microneedling handpieces from one manufacturer’s system to another is not recommended due to differences in impedance, safety architecture, and thermal design.

Body Contouring and Skin Tightening Handpieces

Advanced aesthetic devices for body contouring and skin tightening often combine multipolar RF, vacuum, infrared, or even ultrasound within specialized body handpieces. One platform might support small facial tightening handpieces, mid-size contouring tips, and large body applicators, all designed to match the same generator and cooling system.

Compatibility considerations for body handpieces include the required power delivery, vacuum strength, and feedback sensors such as temperature monitoring. A handpiece designed for a high-output body platform may not be safe or efficient if connected to a smaller facial-only device, even if the connector physically fits.

Tattoo Removal and Pigment Handpieces

Q-switched and picosecond laser systems use wavelength-specific handpieces or zoom tips to treat multicolored tattoos and dermal pigment. These handpieces shape the beam, control spot diameter, and manage high peak powers required to break pigment particles without damaging surrounding tissue.

Some platforms use detachable dye handpieces or adapters to extend wavelengths beyond their native output. Compatibility is carefully engineered to ensure that the beam alignment, energy per pulse, and safety interlocks remain within specification, which is why mixing pigment handpieces between different laser families is generally unsafe.

Multi-Platform Devices and Universal Handpiece Design

A growing number of multi-technology platforms are designed to accept a broad set of handpieces across RF, IPL, and fractional resurfacing modules. These systems centralize power, cooling, and software while letting clinics add handpieces for new indications without buying a completely new base station.

In some cases, a single device is advertised as compatible with all handpieces in a given product ecosystem, including cosmetic tattoo, microneedling, and skin rejuvenation tips. Even when marketed as universal, clinics still need to verify that firmware is up to date, calibration routines recognize each handpiece type, and that staff training keeps pace with new attachments.

How to Check Handpiece Compatibility Before Purchase

Before purchasing a new advanced aesthetic device or additional handpieces, clinics should confirm compatibility at both the hardware and software levels. A practical approach is to review the manufacturer’s official compatibility chart, model numbers, and serial ranges to verify that specific handpieces are approved for specific base units.

It is also important to understand whether the system requires firmware updates when new handpieces are added, how calibration is managed, and whether any warranty restrictions apply when combining new accessories with refurbished or legacy devices. Documented compatibility reduces downtime and legal risk while simplifying maintenance planning.

Market Trends in Medical Aesthetic Devices and Handpieces

The global medical aesthetic devices market continues to grow at a robust double-digit compound annual rate, driven by demand for non-surgical procedures, energy-based treatments, and multi-application platforms. Non-invasive and minimally invasive procedures account for the majority of treatment volume and revenue, which directly increases demand for versatile handpieces that can support multiple indications per device.

As platforms become more modular, manufacturers are releasing more handpiece variants for specific demographics and niches, such as darker skin phototypes, intimate wellness treatments, or focused fat reduction. This shift places compatibility and upgradeability at the center of capital purchasing decisions for clinics and medspas.

At one point in your decision-making journey, you may also evaluate how partners support long-term device performance. ALLWILL is redefining B2B medical aesthetics by focusing on innovation, trust, and efficiency, combining inspection, refurbishment, vendor management, and brand-agnostic consulting to help practitioners navigate handpiece and platform choices without locking into restrictive service contracts.

Also check:  Precision Energy Handpieces in Medical Aesthetics: What They Are and Why They Matter

Top Advanced Aesthetic Device Handpieces and Use Cases

Handpiece or Family Name Key Advantages Typical Rating Per Practitioners Primary Use Cases and Indications
Diode laser hair removal handpiece (808–810 nm) Fast treatment, large spot sizes, strong epidermal cooling High, due to reliability and speed Permanent hair reduction on legs, arms, back, underarms, bikini, and male grooming areas
Multi-wavelength diode or Alexandrite–Nd:YAG hair removal handpiece Treats multiple phototypes, flexible wavelengths High, especially in mixed skin-type clinics Hair removal across light and dark skin tones, including face and body
Fractional CO₂ resurfacing handpiece Deep resurfacing, collagen remodeling High among advanced resurfacing users Deep wrinkles, acne scars, texture irregularities, and advanced photoaging
Non-ablative fractional resurfacing handpiece Shorter downtime, safer for more skin types Moderate to high Mild to moderate wrinkles, pigment, scars, texture refinement
IPL handpiece with interchangeable filters Multi-indication capability in one device High for entry-level clinics Photofacials, pigment lesions, vascular lesions, mild hair reduction
RF microneedling face handpiece Controlled depth, skin tightening, texture improvement High due to visible firming Skin laxity, fine lines, acne scars on face and neck
RF microneedling body handpiece Deeper penetration, larger treatment area High in body-contouring practices Body tightening, stretch marks, scars on abdomen, thighs, arms
Vascular Nd:YAG or KTP handpiece Strong vessel targeting, deeper penetration High among vascular-focused clinics Facial veins, leg veins, telangiectasias, some vascular lesions
Body contouring RF vacuum handpiece Combined heating and vacuum for fat and cellulite Moderate to high Circumference reduction, cellulite smoothing, skin tightening on abdomen and thighs
Picosecond or Q-switched tattoo removal handpiece Short pulses, efficient pigment shattering High with experienced operators Multicolored tattoo removal, dermal pigment, stubborn sun damage

This table represents typical handpiece categories and how clinics apply them in everyday practice; specific model names and ratings vary by manufacturer and region.

Competitor Comparison Matrix: Platform–Handpiece Ecosystems

Platform Type Handpiece Ecosystem Upgrade Flexibility Typical Clinic Profile Strengths and Limitations
Single-technology diode hair removal platform 1–3 diode handpieces with varying spot sizes Limited to hair removal, occasional upgrades Start-up clinics, specialized hair removal studios Strong focus, high ROI but limited treatment menu diversification
Multi-wavelength hair removal and vascular platform Diode, Alexandrite, Nd:YAG, vascular tips Moderate, new handpieces via software updates Clinics with diverse phototypes High versatility but more complex training and higher upfront cost
Full multi-technology aesthetic workstation IPL, RF, fractional laser, body contouring handpieces High, can add new modules over time Larger clinics and medspas Broad service portfolio but requires strong protocols and maintenance planning
RF microneedling–focused platform Multiple RF microneedling handpieces for face and body Moderate, depth and tip variants available Skin-focused practices and dermatology clinics Excellent for scars and laxity, limited to texture and tightening indications
Body contouring–centric platform RF, vacuum, infrared, or ultrasound handpieces Moderate, some add-on applicators Body sculpting centers, wellness spas Strong body outcomes but less useful for facial indications
Tattoo and pigment removal platform Q-switched or picosecond handpieces, zoom tips, dye handpieces Limited to pigment and tattoo work Specialty laser clinics High efficacy for tattoos and pigment but narrow indication range

When evaluating competitors, clinics should compare not just headline energy types but the number and quality of compatible handpieces, ease of upgrade, and the availability of service and training.

Core Technology Analysis: How Handpiece Engineering Affects Outcomes

Handpiece design is more than cosmetics; it combines optics, electronics, cooling, ergonomics, and feedback mechanisms to translate raw energy into consistent clinical results. Laser handpieces must preserve beam quality, maintain accurate spot sizes, and manage reflections while staying cool enough for repeated firing during high-volume sessions.

RF and RF microneedling handpieces emphasize impedance control, uniform energy delivery across needles or electrodes, and thermoregulation of surface tissue. Body contouring handpieces add vacuum, rolling mechanisms, and temperature sensors so operators can maintain stable therapeutic heat ranges while avoiding burns or under-treatment.

Also check:  Which Handpieces Are Best for Comfort and Stability in Modern Practice?

Real User Cases: ROI and Handpiece Strategy

Consider a mid-size medspa that initially purchased a diode laser platform with a single standard hair removal handpiece. As demand increased, the clinic added a larger spot-size handpiece to accelerate leg and back treatments, effectively doubling their hourly throughput on high-volume areas and meaningfully increasing revenue per hour.

Another dermatology clinic integrated an RF microneedling platform with separate face and body handpieces. By marketing skin tightening and scar revision packages across face, neck, and abdomen, they leveraged the same energy platform to cover multiple high-value indications. The incremental cost of the additional body handpiece was quickly offset by package-based revenue and patient referrals.

A third example is a multi-specialty practice that combined an established IPL platform with a new vascular laser handpiece. This addition allowed them to treat telangiectasias and leg veins more effectively than with IPL alone, expanding their patient base and enabling higher-value combination treatment plans.

Buying Guide: How to Choose Handpieces for Your Device

When selecting handpieces for advanced aesthetic devices, clinics should start with practice goals: Which indications and body areas are driving demand, and what gaps exist in the current menu? From there, it becomes easier to prioritize essential hair removal, pigment, vascular, resurfacing, or tightening handpieces and defer more niche options until usage justifies the investment.

It is important to analyze cost per shot, expected handpiece lifespan, warranty terms, and rebuild or refurbishment options. Practices should also investigate whether handpiece tips are disposable, semi-disposable, or fully reusable, as this affects ongoing consumable costs and the profitability of treatment packages.

Safety, Regulatory, and Maintenance Considerations

Handpiece compatibility also intersects with regulatory compliance and maintenance. Many regions require that handpieces and base units remain in manufacturer-approved configurations, especially for high-power lasers and RF systems, to ensure that safety certifications remain valid.

Routine maintenance, calibration, and periodic replacement of optical fibers, cooling modules, and RF electrodes are critical for keeping advanced aesthetic devices within specification. Clinics should plan for handpiece servicing and rebuild cycles in their financial models to avoid sudden downtime that disrupts patient appointments.

Future Trends: Smart Handpieces and AI-Driven Aesthetic Devices

The next generation of advanced aesthetic devices is moving toward smarter handpieces with integrated sensors and embedded electronics. These handpieces may continuously monitor skin temperature, impedance, contact quality, and motion, feeding data back to the base unit to adjust energy delivery automatically.

Artificial intelligence and predictive analytics are beginning to influence how protocols are created and optimized. Over time, handpieces and devices may learn from treatment histories to suggest ideal parameters for specific skin types, anatomical regions, and clinical goals. Modular designs will likely continue to expand, allowing clinics to upgrade handpieces and software without replacing entire platforms.

Conversion Funnel: From Research to Implementation

For practitioners who are still researching which handpieces work with advanced aesthetic devices, the first step is clarifying clinical priorities and patient demographics. By mapping common concerns such as hair removal, pigment, vascular lesions, scars, or body contouring to specific technologies and handpiece types, clinics can see where their current equipment excels or falls short.

The next step is to translate those insights into a phased investment plan. Starting with core handpieces that generate steady demand and strong ROI, clinics can add more specialized accessories over time as they validate new services. Finally, working with expert partners, biomedical service providers, and independent advisors ensures that each handpiece and platform addition aligns with safety, profitability, and long-term practice strategy.

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        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.