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Clinical Handpieces for High-Frequency Treatments: Technologies, Uses, and Buying Guide

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Clinical handpieces for high-frequency treatments sit at the center of modern aesthetic and dermatologic procedures, turning raw device power into precise, safe, and profitable outcomes. In clinics offering radiofrequency skin tightening, RF microneedling, high-frequency ultrasound, helium plasma, or acoustic wave therapy, the handpiece is where energy, ergonomics, and treatment protocols converge.

What Are Clinical Handpieces for High-Frequency Treatments?

Clinical handpieces for high-frequency treatments are the applicators attached to energy-based aesthetic devices that deliver radiofrequency, ultrasound, plasma, or high-frequency mechanical waves into tissue. They define how deeply energy penetrates, how evenly it is distributed, and how comfortable a treatment feels to the patient.

In radiofrequency-based aesthetic systems, the handpiece may contain monopolar, bipolar, or multipolar electrodes that heat the dermis and subcutaneous tissue for skin tightening and contouring. In RF microneedling devices, the handpiece integrates insulated or non-insulated needles, pulse control, and sometimes cooling, enabling fractional treatment of skin texture, scars, and wrinkles. For high-frequency ultrasound or acoustic wave platforms, the handpiece houses transducers or vibration components that control frequency, focal depth, and power to stimulate collagen or improve lymphatic drainage and circulation.

High-Frequency Energy Modalities and Handpiece Design

High-frequency treatments span several energy modalities, each requiring specific handpiece architecture to perform safely and predictably.

Radiofrequency handpieces are designed to deliver alternating current at frequencies that generate controlled thermal effects by tissue resistance. They can be contact-based, using electrodes that glide over conductive gel, or minimally invasive, using probes or needles to heat subdermal layers. The geometry of electrodes, contact surface area, and cooling mechanisms determine how uniformly the tissue reaches therapeutic temperature.

RF microneedling handpieces combine mechanical needle insertion with RF energy delivery. The needles puncture the skin to a controlled depth, then RF pulses heat the surrounding tissue, promoting neocollagenesis and skin remodeling. Needle density, needle coating, pulse duration, and feedback on impedance or temperature are key differentiators that influence downtime and outcomes.

High-frequency ultrasound handpieces, especially at dermatologic frequencies around 20 MHz, use focused acoustic energy to create precise thermal lesions in the epidermis and upper dermis without damaging adjacent structures. Focal depth, spot size, and acoustic coupling through gel directly affect the safety and accuracy of lesion placement for indications like seborrheic keratosis and superficial lesions.

Helium plasma and RF hybrid handpieces deliver radiofrequency energy into ionized helium gas to produce a focused plasma stream capable of cutting, coagulating, or contracting soft tissue. These handpieces must balance energy density with thermal spread, making tip design, plasma flow, and RF control critical, especially in subcutaneous applications such as post-liposuction skin contraction.

High-frequency vibration and acoustic wave handpieces generate mechanical oscillations, often in the range up to around 50 Hz for body treatments, used to stimulate lymphatic flow, neuromuscular activation, and microcirculation. The handpiece typically incorporates ergonomic grips and interchangeable applicators designed for different body regions and tissue depths.

Clinical Handpieces vs. Base Consoles

In platform systems, the console houses the generator, software, and user interface, while the clinical handpiece acts as the treatment endpoint. For radiofrequency-based aesthetic device markets, platform consoles account for a majority of system value, yet handpieces drive customization and procedure diversity.

Platform systems often support multiple handpieces with different energy modes, needle configurations, or focal depths. A single console may run:

Face-specific RF microneedling handpieces with smaller footprints and shallow depth settings
Body-focused RF handpieces with higher maximum energy and integrated cooling
Precision single-needle handpieces for periorbital, perioral, or submental regions
Plasma or electrosurgical handpieces for subdermal tightening

Because handpieces are replaced more frequently than consoles, they represent a recurring revenue stream and an important factor in the total cost of ownership. Practices must consider consumable needle tips, disposable electrodes, and maintenance cycles when evaluating profitability.

Applications of High-Frequency Handpieces in Aesthetic Medicine

Clinical handpieces for high-frequency treatments support a wide spectrum of aesthetic and dermatologic applications. Skin tightening via radiofrequency handpieces uses controlled dermal heating to stimulate collagen contraction and neocollagenesis, improving mild to moderate laxity on the face, neck, jawline, and body. RF microneedling handpieces are widely used for acne scars, surgical scars, fine lines, crepey skin, and enlarged pores, where fractional injury and RF thermal coagulation lead to smoother texture and improved tone.

High-frequency ultrasound handpieces with superficial focal depths can precisely treat benign lesions such as superficial keratoses by creating localized coagulation zones in the upper dermis. Acoustic wave and high-frequency vibration handpieces support body contouring protocols by enhancing microcirculation, accelerating lymphatic drainage, and reducing tissue stiffness, often as part of a combined protocol with shockwave or vacuum technologies.

Helium plasma and RF hybrid handpieces provide minimally invasive tissue contraction in subcutaneous planes, used in conjunction with liposuction or as standalone skin tightening in regions like the neck and submental area. These applications highlight how handpiece design dictates dose control, safety margins, and the ability to treat anatomically challenging zones.

Market Trends: High-Frequency Aesthetic Handpieces

The global radiofrequency-based aesthetic devices market has been expanding at a double-digit compound annual growth rate, driven by demand for non-surgical skin tightening, scar revision, and body contouring. Industry analyses for 2024 and beyond estimate market values in the range of over one and a half billion dollars, with projections surpassing three to four billion dollars over the next decade as RF-based treatments become more mainstream and accessible.

North America holds the largest share of the radiofrequency-based aesthetic device market, reflecting high patient awareness and strong adoption of premium RF microneedling platforms in medical spas and dermatology practices. At the same time, Asia-Pacific is expected to grow at the fastest pace, as clinics respond to demand for non-invasive and minimally invasive rejuvenation with devices optimized for diverse skin types and phototypes.

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High-frequency handpieces benefit from this trend because clinics are shifting from single-application devices toward multi-handpiece platforms that can address everything from texture to laxity with one energy source. The push for shorter downtimes and more comfortable procedures is also fueling innovation in handpiece cooling, real-time feedback, and smarter pulse delivery.

Core Technology: Radiofrequency Handpieces

Radiofrequency handpieces convert RF generator output into controlled tissue heating by leveraging tissue impedance. Monopolar RF handpieces use one active electrode at the tip and a return pad elsewhere on the body, allowing deeper and more diffuse heating ideal for skin laxity and body contouring. Bipolar and multipolar handpieces place both electrodes in the treatment area, confining current paths and offering more superficial, precise heating, which suits delicate areas and fine lines.

Temperature control is central to modern RF handpiece design. Some handpieces incorporate contact cooling plates, cryogen spray, or real-time temperature sensors to maintain epidermal safety while driving dermal temperatures to ranges that induce collagen denaturation and remodeling. Treatment parameters like pulse duration, duty cycle, and stacking of shots can be adjusted to balance efficacy with patient comfort.

Electrode materials and surface finishes affect energy dispersion and risk of arcing or hotspots, especially at higher power settings. Handpieces designed for long procedures must be lightweight, well-balanced, and thermally insulated to reduce operator fatigue. Cable flexibility, handpiece swivel joints, and autoclavable or disinfectable surfaces form part of the practical engineering that determines everyday usability.

Core Technology: RF Microneedling Handpieces

RF microneedling handpieces have become central to many high-frequency treatment portfolios because they can address both textural and tightening concerns in a controlled, fractional manner. The handpiece typically contains:

A cartridge of insulated or non-insulated needles
A motorized mechanism for depth control and needle deployment
RF circuitry that delivers energy only when needles are inserted into tissue
Settings for pulse duration, power, and number of pulses per insertion

Insulated needles confine energy to the tips, reducing epidermal heating and lowering risk of post-inflammatory hyperpigmentation, while non-insulated needles deliver energy along the shaft, increasing coagulation volume. Depth ranges can span from fractions of a millimeter for epidermal rejuvenation to several millimeters for deeper scarring or body treatments.

Advanced RF microneedling platforms offer multiple handpieces tailored to specific uses, such as face, delicate areas, or body. One handpiece may feature a 36-needle array for larger areas like the cheeks and forehead, while another offers a single needle for focal lesions or periorbital wrinkles. Integrated cooling plates and vacuum-assisted needle insertion can improve comfort and consistency, especially at higher energy levels.

High-Frequency Ultrasound and Acoustic Handpieces

High-frequency ultrasound handpieces, particularly those operating at dermatologic frequencies around 20 MHz, create precisely focused thermal lesions at controlled depths in the skin. By selecting handpieces with different nominal focal depths, practitioners can target the epidermis, upper dermis, or deeper dermal layers without affecting underlying structures. Acoustic coupling through gel and real-time visualization via integrated imaging or dermoscopy make these handpieces powerful tools for lesion removal and targeted rejuvenation.

High-frequency vibration and acoustic wave handpieces bring a different type of energy to aesthetic protocols. Devices that reach oscillation speeds around 50 Hz can be used for lymphatic activation at lower frequencies and neuromuscular and vascular activation at higher frequencies, supporting tissue toning, post-treatment recovery, and relief of muscular tension. The ability to customize frequencies and protocols through the handpiece enhances versatility in body shaping and wellness-oriented treatments.

Helium Plasma and Electrosurgical RF Handpieces

Helium plasma RF handpieces are designed for subcutaneous dermatologic and aesthetic procedures where controlled tissue contraction and coagulation are required. They use helium gas energized by RF current to produce a focused plasma stream that delivers energy efficiently with limited thermal spread. This allows surgeons and cosmetic physicians to contract subcutaneous tissues in areas like the neck or lower face, often in combination with liposuction for contour enhancement.

These handpieces typically connect to multipurpose electrosurgical consoles that provide monopolar, bipolar, and helium plasma modes. Tip design, energy profiles, and safety interlocks are crucial, especially when working near critical structures. The indication set often includes the improvement of lax skin in specific regions, and the ability to use the same console for both cutting and coagulation makes these handpieces valuable in multidisciplinary practices.

Ergonomics, Safety, and Infection Control

No discussion of clinical handpieces for high-frequency treatments is complete without addressing ergonomics and safety. Practitioners may perform multiple procedures per day, so handpieces must minimize strain while enabling precise control around complex anatomical curves. Lightweight construction, balanced center of gravity, and textured grips help reduce fatigue, especially when treating large body areas.

Safety features include built-in temperature monitoring, impedance feedback, and energy cutoffs when contact is lost or resistance is outside the target range. Some handpieces integrate visual or audible cues to indicate when tissue has reached the desired therapeutic endpoint, supporting reproducible outcomes across operators. For RF microneedling and invasive RF or plasma handpieces, single-use tips and sterile packaging are essential to minimize infection risk.

Infection control also extends to how easily the handpiece body can be cleaned and disinfected. Smooth surfaces, limited crevices, and compatibility with standard disinfectants help ensure compliance with clinic protocols. Autoclavable or high-level disinfectable components may be required for handpieces used in more invasive or surgical contexts.

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Company Solutions and Ecosystem Support

Within this landscape, service and lifecycle management of high-frequency handpieces have become as important as the underlying technology. ALLWILL is redefining B2B medical aesthetics by offering brand-agnostic consultations, a Smart Center for inspection and refurbishment, and tools like MET and Lasermatch that connect clinics with vetted technicians, trainers, and optimized device sourcing. For clinics expanding RF or high-frequency offerings, this type of ecosystem support helps reduce downtime, extend handpiece lifespan, and control total cost of ownership.

ROI and Practice Economics of High-Frequency Handpieces

When clinics evaluate clinical handpieces for high-frequency treatments, the decision is rarely about technology alone; it is about return on investment and practice integration. RF microneedling and RF skin tightening procedures often command premium pricing, with typical packages involving three to four sessions per patient. By forecasting utilization, a clinic can estimate payback periods that range from a few months to a couple of years, depending on patient volume and consumable costs.

Disposable needle tips, single-use electrodes, and cartridges directly affect margins. Systems with flexible handpiece options allow clinics to tailor offerings to different price points—basic skin tightening, premium combined RF microneedling and PRP, or advanced plasma-assisted tightening—without investing in multiple consoles. Training requirements, learning curves, and marketing support from manufacturers or partners can accelerate adoption and help practitioners position high-frequency treatments within their portfolios.

Real-World Use Cases and Treatment Pathways

Real user cases highlight how clinical handpieces for high-frequency treatments translate into practical outcomes. A dermatology clinic might deploy an RF microneedling handpiece to treat atrophic acne scars in patients who previously failed topical regimens, achieving visible improvement after three sessions spaced four to six weeks apart. Combining high-frequency RF microneedling with topical growth factors can further enhance texture and tone in photoaged skin.

A plastic surgery practice may use a helium plasma RF handpiece following liposuction in the neck and lower face to provide additional tightening, reducing the need for more invasive lifting procedures in select patients. In another scenario, a med spa uses high-frequency vibration and acoustic wave handpieces as part of a body contouring protocol to speed recovery and reduce post-treatment discomfort after shockwave or cryolipolysis sessions.

These case pathways underscore the value of matching handpiece type, energy modality, and protocol design to patient goals, downtime tolerance, and risk profile. Clinics that carefully document before-and-after results and patient satisfaction can refine protocols and optimize pricing to maximize both outcomes and profitability.

Top Clinical Handpiece Categories and Use Cases

Handpiece Category Key Advantages Typical Ratings Sentiment Common Use Cases
RF skin tightening handpiece Non-surgical lifting, suitable for multiple skin types, moderate downtime High satisfaction for mild to moderate laxity Face and neck tightening, jawline contouring, body skin firmness
RF microneedling handpiece (multi-needle) Texture and scar improvement, customizable depth and energy Strong ratings for scars and wrinkles Acne scarring, fine lines, large pores, stretch marks
Precision RF microneedling handpiece (single needle) Targeted treatment of delicate areas, high control Positive feedback for focal wrinkles Periorbital lines, perioral lines, localized scars
High-frequency ultrasound handpiece Precise focal depth, minimal collateral damage Favorable for lesion treatment Superficial benign lesions, localized rejuvenation
Helium plasma RF handpiece Subcutaneous tissue contraction, adjunct to liposuction High impact in body contour cases Neck and submental tightening, body contouring adjunct
Acoustic and vibration handpiece Lymphatic stimulation, comfort enhancement Good acceptance in body protocols Post-body contouring recovery, tissue toning, lymphatic support

Competitor Comparison Matrix for High-Frequency Handpiece Platforms

Platform Focus Handpiece Variety Key Technology Strengths Practice Fit
Dedicated RF microneedling systems Multiple needle arrays and precision tips Fractional RF with depth control, tailored for texture and scars Dermatology and med spas focused on rejuvenation
RF skin tightening consoles Multiple RF modes, contact cooling handpieces Non-invasive tightening with strong safety features Clinics prioritizing minimal downtime tightening
Combined RF and plasma consoles RF and helium plasma handpieces on one base Versatile cutting, coagulation, and tissue contraction Plastic surgery and advanced aesthetic practices
Ultrasound-focused platforms Multiple focal depth handpieces High-frequency focused ultrasound for lesions and tightening Dermatologists and clinics with lesion workflows
Acoustic wave and vibration systems Massage and vibration handpieces Lymphatic and neuromuscular activation, body treatment support Body contouring centers and wellness clinics

How to Select Clinical Handpieces for High-Frequency Treatments

Selecting the right clinical handpieces begins with a clear definition of service lines. Clinics must ask whether their priority is non-invasive facial tightening, comprehensive scar and texture work, minimally invasive body contouring, or lesion treatment. RF microneedling handpieces are ideal for texture and scars, while monopolar RF handpieces excel in skin laxity, and plasma or ultrasound handpieces may be better suited for localized lesions.

Patient demographics and skin types strongly influence device choice. Practices serving a diverse range of Fitzpatrick phototypes may favor handpieces with insulated needles, robust epidermal cooling, and adjustable energy to minimize hyperpigmentation risk. High-frequency handpieces that support real-time temperature or impedance monitoring help standardize treatment endpoints, especially in high-volume med spa environments.

Operational considerations include compatibility with existing consoles, availability of local service and training, and total cost of ownership over the expected lifespan. Handpiece durability, warranty terms, and access to refurbished or replacement units can significantly affect uptime. Clinics should also weigh user interface design and how easily staff can transition between different handpieces and protocols during a busy day.

Best Practices for Using High-Frequency Handpieces Safely

Safe use of clinical handpieces for high-frequency treatments depends on a combination of device design and practitioner technique. Proper patient selection and thorough medical history help identify contraindications such as implanted devices, active infections, or certain systemic conditions. Pre-treatment skin preparation, including cleansing and removal of makeup or topical agents, reduces the risk of adverse reactions.

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Practitioners should begin with conservative settings, particularly for patients with darker skin tones or new indications, and adjust energy and pass count based on real-time feedback. Uniform handpiece movement, consistent contact with the skin, and overlap patterns recommended by the manufacturer support even energy distribution. Cooling strategies, whether integrated or manual, can enhance comfort and protect the epidermis during higher-energy passes.

Post-treatment care often involves soothing topicals, sun protection, and clear instructions regarding downtime and expected reactions. For RF microneedling, patients may experience transient erythema and edema, while for subcutaneous RF or plasma treatments, swelling and tenderness are more pronounced and should be discussed beforehand. Documenting parameters and results creates a feedback loop that refines protocols and helps train new team members.

Regulatory and Compliance Considerations

Clinical handpieces for high-frequency treatments are typically regulated as medical devices or components, and their indications for use depend on regional approvals. Practices must ensure that devices and handpieces are cleared or approved for their intended applications, whether that is wrinkle reduction, skin resurfacing, treatment of benign lesions, or subcutaneous tissue coagulation.

Labels, user manuals, and official indications provide guidance on safe treatment parameters and contraindications. Using handpieces outside of their indicated use can increase risk and may expose clinics to regulatory or legal liability. Proper staff training, documentation of informed consent, and adherence to manufacturer maintenance schedules form the foundation of compliant operation.

Future Trends in High-Frequency Handpiece Technology

The future of clinical handpieces for high-frequency treatments is moving toward greater personalization, automation, and integration with digital tools. Next-generation handpieces are increasingly incorporating real-time temperature mapping, impedance-based energy modulation, and AI-assisted settings that adjust energy output to maintain consistent tissue response across different anatomical zones.

Multi-energy handpieces that combine RF with additional modalities, such as optical energy, vacuum, or ultrasound, may continue to grow, enabling multi-layered treatments in a single pass. Needle technologies in RF microneedling are evolving toward more durable, sharper, and potentially robotically guided arrays that reduce discomfort and variability between operators.

Sustainability and cost efficiency are also emerging as design priorities. Handpieces that balance longevity with smart, lower-cost consumables can help clinics meet environmental goals while protecting margins. As non-invasive and minimally invasive aesthetics remain in high demand, clinical handpieces for high-frequency treatments will continue to be refined for comfort, safety, and performance.

FAQs on Clinical Handpieces for High-Frequency Treatments

What are clinical handpieces for high-frequency treatments?
Clinical handpieces for high-frequency treatments use controlled electrical energy to stimulate skin renewal, collagen production, and healing. They allow precise energy delivery, minimizing discomfort and downtime while improving treatment accuracy and outcomes for practitioners and patients.

How is high-frequency handpiece technology evolving?
High-frequency handpiece technology is advancing with smarter controls, AI integration, and better thermal management. These innovations enhance energy precision, extend device life, and improve patient safety, allowing clinics to deliver faster, more effective aesthetic treatments.

How should you choose the best clinical handpieces?
Select handpieces based on treatment type, frequency range, durability, and maintenance support. Evaluate materials, ergonomics, and compatibility with existing systems. Purchasing from trusted providers ensures sustained performance, technical support, and compliance with medical standards.

How do you maintain clinical handpieces for longevity?
Regular cleaning, calibration, and inspection are key. Always follow manufacturer protocols, use recommended disinfectants, and schedule preventive maintenance. Proper handling and storage significantly extend the lifespan and reliability of your clinical handpieces.

What are the main uses of high-frequency clinical handpieces?
They are primarily used for skin tightening, acne treatment, collagen remodeling, and wound healing. These devices deliver controlled microcurrents that enhance tissue regeneration and support non-invasive aesthetic and dermatologic procedures.

Who are the most trusted vendors for clinical handpieces?
Reliable vendors offer verified devices, transparent pricing, and technical training support. ALLWILL stands out by connecting clients with vetted technicians and streamlined procurement systems, ensuring consistent quality and operational confidence across equipment lines.

Why consider refurbished clinical handpieces for your clinic?
Refurbished clinical handpieces reduce upfront costs while maintaining high performance. Delivered through certified facilities, they undergo strict functionality checks and testing, offering excellent value for clinics aiming to balance performance and affordability.

What are the future trends in clinical handpieces?
Future clinical handpieces will feature real-time energy monitoring, improved cooling, and ergonomic designs. Integration with AI platforms will optimize treatments by adjusting parameters automatically, increasing efficiency, and ensuring consistent patient outcomes.

Conversion-Focused Pathways for Clinics

Clinics just starting with high-frequency treatments can begin by adding a versatile RF microneedling handpiece that addresses common concerns like scars, wrinkles, and texture, building a patient base and before-and-after gallery. Once these core services gain traction, adding dedicated RF skin tightening or acoustic wave handpieces allows expansion into non-invasive lifting and body contouring support with minimal disruption to workflows.

Established practices looking to differentiate can explore helium plasma or high-frequency ultrasound handpieces to tackle more advanced cases, post-liposuction tightening, or lesion-focused work, positioning themselves as comprehensive centers for energy-based aesthetic medicine. By aligning clinical handpiece selection with patient demographics, marketing strategy, and long-term ROI targets, clinics can transform high-frequency treatments into a sustainable growth engine for their business.

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

(c) Limited Warranties, If Any.

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

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

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

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

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

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

        12. PROPRIETARY RIGHTS.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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