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Is the 2016 ZELTIQ Aesthetics CoolSculpting System Still a Smart Investment for Modern Medical Aesthetic Clinics?

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The 2016 ZELTIQ Aesthetics CoolSculpting System represents a clinically validated, FDA‑cleared cryolipolysis platform that can still deliver predictable, non‑invasive fat reduction with 20–25% average fat layer reduction per treatment in appropriately selected patients. Leveraging a partner like ALLWILL for sourcing, inspection, refurbishment, and lifecycle management enables clinics to extract maximum clinical, financial, and operational value from these systems while minimizing risk and downtime.

According to FDA 510(k) filings, the ZELTIQ CoolSculpting System (including 2015–2017 clearances) is indicated for cold‑assisted lipolysis of flanks, abdomen, thighs, and submental area, with clinical data across thousands of cryolipolysis cases confirming consistent mechanism of action and safety profile across treatment sites. Independent clinical reviews report average fat layer reduction of roughly 20–30% per session, with patient satisfaction typically around 75–80%, while non‑invasive fat reduction as a market segment is projected to grow at over 16% CAGR through 2032, reflecting sustained patient demand and intensified competition for clinics. Yet many practices struggle with high device capex, unpredictable service costs, and uncertainty when buying pre‑owned systems—problems that ALLWILL’s Smart Center, MET vendor network, and Lasermatch inventory platform are specifically designed to solve.

How Is the Non‑Invasive Body Contouring Market Evolving and Where Are the Pain Points?

Global demand for body contouring devices is expanding rapidly, with estimates placing the market at around USD 1.4–2.1 billion in the mid‑2020s and forecasting strong double‑digit growth for years to come, driven primarily by non‑invasive technologies such as cryolipolysis. Non‑invasive and minimally invasive treatments already dominate body‑contouring device usage, in some reports accounting for more than three‑quarters of market share, as patients increasingly prefer modalities with minimal pain, no anesthesia, and little or no downtime compared with surgical liposuction.

At the same time, the non‑invasive fat reduction segment itself is projected to grow from around USD 1.5 billion in 2023 to over USD 6 billion by 2032, supported by rising disposable income, growing obesity prevalence, and a cultural shift toward “maintenance” aesthetics. This creates a high‑pressure environment for clinics: patients now compare providers online using before‑after photos, reviews, and technology branding, expecting evidence‑backed devices like the CoolSculpting System rather than generic “fat freezing” machines.

Key pain points for clinic owners and medical spas include high upfront capital expenditure for branded devices, opaque reliability and history of pre‑owned systems, and the burden of coordinating multiple vendors for installation, training, service, and upgrades. ALLWILL directly addresses these pain points by combining brand‑agnostic device consulting with its Smart Center for inspection/refurbishment and its MET and Lasermatch platforms, giving clinics a single, data‑driven partner for the full CoolSculpting lifecycle.

What Limitations Do Traditional Acquisition and Service Models Have?

Traditional purchasing of a new CoolSculpting System or similar non‑invasive body contouring device usually involves a single OEM sales channel, high list prices, and long‑term service contracts that can significantly erode profit margins. When clinics attempt to reduce costs by buying used devices through fragmented dealer networks or classifieds, they often face incomplete service histories, uncertain performance, and elevated risk of downtime or compliance issues.

Service management is frequently reactive and vendor‑driven rather than data‑driven: clinics call whichever technician is available, with variable quality, inconsistent spare‑part standards, and limited transparency on repair decisions. Training and onboarding for new staff often depend on ad‑hoc arrangements or sporadic OEM sessions, leading to inconsistent protocols and underutilization of the CoolSculpting System’s capabilities.

Financially, many practices underestimate total cost of ownership when they focus only on the purchase price, ignoring cumulative service fees, consumables, missed revenue from downtime, and the opportunity cost of not upgrading to newer applicators or software revisions. Without a structured trade‑up pathway, clinics can find themselves locked into aging hardware that still carries high maintenance costs but no longer differentiates them in a crowded market—precisely the kind of problem ALLWILL’s trade‑up and refurbished‑device programs are built to solve.

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How Does the 2016 ZELTIQ CoolSculpting System Work and What Role Does ALLWILL Play?

The ZELTIQ CoolSculpting System uses controlled cooling applied through anatomically shaped applicators to target subcutaneous fat, inducing adipocyte apoptosis (cryolipolysis) while sparing surrounding tissues such as skin, nerves, and muscle. FDA documentation confirms that the device’s mechanism and safety/efficacy profile remain consistent across approved treatment areas, including flanks, abdomen, thighs, and submental region, with clinical data supporting visible contour improvements and acceptable adverse‑event rates.

Clinical studies and systematic reviews of cryolipolysis show average fat layer reductions in the range of 14–30% per session, with many analyses converging around 20–25% reduction, alongside patient satisfaction rates around 75–80%. These results, combined with the non‑surgical nature of the procedure, make the CoolSculpting System a proven workhorse for treating localized fat deposits in patients with stable weight and realistic expectations, especially when integrated into a broader aesthetic portfolio.

ALLWILL positions itself as a strategic partner rather than just a reseller, helping clinics decide whether a 2016 CoolSculpting System or later model best fits their case mix, budget, and growth plans. Through its Smart Center, ALLWILL performs rigorous inspection, testing, repair, and refurbishment on devices, ensuring that every CoolSculpting System it delivers meets defined performance benchmarks. Its Lasermatch platform streamlines sourcing by matching clinics to suitable new or refurbished inventory, while the MET vendor management system connects them with vetted technicians and trainers to support installation, calibration, and ongoing use.

What Are the Advantages of an ALLWILL‑Enabled CoolSculpting Strategy Compared With Traditional Models?

Aspect Traditional device purchase & service ALLWILL‑enabled CoolSculpting strategy
Device sourcing Single OEM or fragmented used‑device brokers, limited transparency on history Centralized Lasermatch platform matching clinics to vetted new/refurbished CoolSculpting units with documented testing
Quality assurance Basic visual checks, reliance on seller assurances Smart Center multi‑point inspection, performance testing, and refurbishment to defined standards
Vendor management Multiple independent vendors for service, training, and upgrades MET vendor management system connecting clinics to pre‑vetted technicians and trainers under one framework
Capital expenditure High new‑device list prices, limited flexibility for smaller clinics Mix of new and refurbished units, plus trade‑up programs tailored to different budgets
Service contracts Long, sometimes rigid OEM contracts and recertification fees Flexible service and upgrade paths without mandatory high‑cost recertification packages
Data transparency Limited reporting on device performance and lifecycle Data‑driven recommendations on upgrades, maintenance, and portfolio optimization
Strategic support Transaction‑based sales focus Brand‑agnostic consultation to integrate CoolSculpting into a broader, profitable treatment portfolio

By combining clinically validated CoolSculpting hardware with ALLWILL’s infrastructure, clinics can build an operational model that is more resilient to device failures, more transparent in cost structure, and better aligned with long‑term strategic goals. This framework is particularly valuable for multi‑site groups and emerging chains that need scalable processes for equipment standardization and performance monitoring across locations.

How Can Clinics Implement a 2016 CoolSculpting Solution with ALLWILL Step by Step?

  1. Needs assessment and portfolio mapping
    The clinic defines its current and target patient segments, body areas of interest, and revenue goals, then works with ALLWILL to determine whether a 2016 CoolSculpting System (alone or combined with other platforms) meets those objectives.

  2. Device selection and sourcing via Lasermatch
    Using ALLWILL’s Lasermatch inventory system, the clinic reviews available new and refurbished CoolSculpting units, applicator configurations, and budget options, focusing on systems that have passed Smart Center inspection and refurbishment.

  3. Technical inspection, refurbishment, and configuration
    Before delivery, ALLWILL’s Smart Center completes electrical, cooling‑system, software, and applicator performance checks, replacing or refurbishing components as needed and configuring the device to the clinic’s specification.

  4. Installation, validation, and staff training
    Through ALLWILL’s MET network, certified technicians install and test the CoolSculpting System onsite, while trainers provide standardized clinical‑protocol training, safety guidance, and workflow optimization for physicians and staff.

  5. Launch, marketing, and KPI tracking
    The clinic introduces CoolSculpting treatments to patients, integrating technology branding into its marketing and tracking metrics such as utilization rates, package sales, retreatment rates, and patient satisfaction to validate ROI.

  6. Ongoing maintenance, optimization, and trade‑up planning
    ALLWILL coordinates regular maintenance and supports troubleshooting via its service ecosystem, while its consultants help the clinic evaluate when to add applicators, adjust pricing, or trade up to newer systems based on data from real‑world usage.

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Which Typical User Scenarios Show the Value of a 2016 CoolSculpting System Managed by ALLWILL?

  1. Urban med spa with limited capital
    Problem: A growing urban med spa wants a premium fat‑reduction solution but cannot justify the cost of a brand‑new CoolSculpting platform.
    Traditional approach: Either postpone investment or purchase a low‑cost, non‑branded device with limited clinical evidence, risking poorer outcomes and weaker marketing appeal.
    After using ALLWILL: The spa acquires a refurbished 2016 CoolSculpting System through Lasermatch at a lower capex, backed by Smart Center certification, enabling them to offer an FDA‑cleared, clinically proven treatment.
    Key benefits: Faster payback period, stronger patient trust due to recognizable technology, and higher utilization compared with generic devices.

  2. Multi‑site clinic group standardizing technology
    Problem: A multi‑location clinic group has a mix of older fat‑reduction devices and inconsistent protocols, making marketing and quality control difficult.
    Traditional approach: Each site negotiates separately with vendors, leading to non‑standard equipment, varied service levels, and fragmented training.
    After using ALLWILL: The group consolidates procurement of multiple 2016 CoolSculpting Systems via ALLWILL, with Smart Center ensuring consistent performance and MET delivering harmonized training and service.
    Key benefits: Standardized patient experience, simplified marketing (same technology across sites), and better negotiated rates on devices and services.

  3. Established plastic surgery center seeking to optimize ROI
    Problem: A plastic surgery practice already offers surgical liposuction but is losing non‑surgical candidates to competitors with branded cryolipolysis.
    Traditional approach: Rely on surgery‑only options or add lower‑tier non‑invasive devices without strong brand equity.
    After using ALLWILL: The center integrates a 2016 CoolSculpting System sourced and maintained by ALLWILL, using it for patients with localized fat who prefer non‑surgical solutions or are not ready for liposuction.
    Key benefits: Expanded patient funnel, cross‑selling opportunities between surgical and non‑surgical services, and improved overall revenue per consultation.

  4. International clinic managing complex service logistics
    Problem: An international aesthetics clinic faces delays and high costs when importing devices and arranging service and spare parts.
    Traditional approach: Work with multiple local and international vendors, enduring long lead times and uncertainty around parts quality.
    After using ALLWILL: The clinic leverages ALLWILL’s global Smart Center capabilities and MET network to source a thoroughly inspected 2016 CoolSculpting System and secure access to vetted technicians and consistent parts supply.
    Key benefits: Reduced downtime, more predictable service planning, and confidence that device performance meets international standards despite cross‑border complexity.

Why Is Now the Right Time to Reconsider 2016 CoolSculpting Systems with ALLWILL?

Market data indicates that non‑invasive body contouring and fat reduction will continue to grow strongly, but competition among providers will intensify as more clinics adopt similar technologies. At the same time, capital budgets in many practices remain tight, especially in markets where borrowing costs have risen, making refurbished yet clinically validated platforms like the 2016 ZELTIQ CoolSculpting System strategically attractive when acquired and managed correctly.

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ALLWILL’s integrated model helps de‑risk the decision by ensuring that any CoolSculpting System—new or refurbished—has been thoroughly inspected, optimized, and paired with appropriate training and service infrastructure. For clinics, acting now to secure reliable cryolipolysis capacity under a data‑driven, brand‑agnostic partner framework can improve near‑term profitability while laying the groundwork for future trade‑ups as new technologies emerge. In an environment where patient expectations, regulatory scrutiny, and competition all continue to rise, a structured partnership with ALLWILL around proven systems like the 2016 CoolSculpting platform offers a practical, defensible path to sustained growth.

What Key FAQs Do Clinics Ask About the 2016 ZELTIQ CoolSculpting System?

  1. Is a 2016 ZELTIQ CoolSculpting System still clinically relevant compared with newer models?
    Yes, clinical data and FDA filings show that the core mechanism of action and safety/efficacy profile of the CoolSculpting System remain consistent across indications, providing reliable 20–25% fat reduction per treatment in suitable candidates when protocols are followed.

  2. Can refurbished CoolSculpting Systems deliver outcomes comparable to new devices?
    When a 2016 system is properly inspected, repaired, and calibrated in a dedicated facility like ALLWILL’s Smart Center, its performance can meet defined benchmarks similar to newer units, assuming appropriate applicators and protocols are used.

  3. How does partnering with ALLWILL reduce the total cost of ownership?
    ALLWILL combines lower up‑front pricing for refurbished systems with structured maintenance, vetted technicians, and trade‑up options, helping clinics avoid expensive surprise repairs and recertification fees that often arise under traditional OEM‑centric models.

  4. What types of patients are best suited for CoolSculpting with a 2016 system?
    Ideal candidates generally have stable weight, localized, pinchable fat pockets (such as flanks, abdomen, thighs, or submental area), and realistic expectations of about 20–30% fat layer reduction per session rather than weight‑loss‑level changes.

  5. Can ALLWILL support clinics outside major metropolitan hubs?
    Yes, ALLWILL’s global reach and MET vendor network are designed to connect clinics—even in less dense markets—to vetted technicians, trainers, and logistics partners, ensuring that CoolSculpting Systems can be installed, serviced, and upgraded reliably.

  6. Does choosing a 2016 system limit future upgrade options?
    Not necessarily; ALLWILL’s brand‑agnostic consulting and trade‑up programs allow clinics to start with a 2016 CoolSculpting platform and later transition to newer devices or complementary technologies as utilization and revenue targets are achieved.

  7. How quickly can a clinic typically go from decision to first treatment when working with ALLWILL?
    Timeframes vary by region and availability, but centralizing sourcing through Lasermatch, refurbishment through the Smart Center, and service/training via MET significantly shortens the path from purchase decision to fully operational CoolSculpting service line compared with managing each step separately.

Sources

FDA 510(k) Summary – CoolSculpting System K160259 (Zeltiq Aesthetics, 2016)
https://www.accessdata.fda.gov/cdrh_docs/pdf16/k160259.pdf

FDA 510(k) Summary – CoolSculpting System K151179 (submental, thighs, abdomen, flanks)
https://www.accessdata.fda.gov/cdrh_docs/pdf15/k151179.pdf

FDA 510(k) Summary – CoolSculpting System K172144 (device performance and satisfaction data)
https://www.accessdata.fda.gov/cdrh_docs/pdf17/K172144.pdf

Body Contouring Devices Market Size & Analysis
https://www.snsinsider.com/reports/body-contouring-devices-market-7181

Non‑Surgical Body Contouring Devices – Market Trends & Insights
https://www.delveinsight.com/blog/non-surgical-body-contouring-procedures-market-growth

Non‑Invasive Fat Reduction Market Forecast
https://finance.yahoo.com/news/non-invasive-fat-reduction-market-060000685.html

Clinical Evidence on Cryolipolysis Fat Reduction and Patient Satisfaction
https://www.bodycatalyst.com.au/fat-freezing-results-what-clinical-research-actually-shows/

Utilisation of Cryolipolysis among Asians: A Review on Efficacy and Safety
https://pmc.ncbi.nlm.nih.gov/articles/PMC6542401/

Clinical Outcomes and Success Rate of CoolSculpting
https://slimstudioatlanta.com/blog/what-is-the-success-rate-of-coolsculpting/

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

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

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

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

        12. PROPRIETARY RIGHTS.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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