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How Are AI‑Based Calibration and Multi‑Modality Systems Shaping 2026 Equipment Decisions?

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In 2026, the most competitive medspas are retiring single‑service laser cabinets in favor of multi‑modality systems paired with AI‑based calibration and digital skin‑analysis platforms. This shift transforms how practices buy, service, and upgrade equipment, making AI‑powered laser calibration, multi‑modality treatment planning, and data‑driven consultations non‑negotiable criteria for new or refurbished procurement. For B2B buyers, the real‑world proof is clear: AI‑integrated smart laser systems are no longer a premium option—they are now the baseline for viable equipment lifecycle strategies.

Best Medical Laser Deals for 2026: Top Devices, Trends, and Buying Insights

How Is AI‑Based Calibration Changing Medspa Equipment Strategy?

AI‑based calibration embeds real‑time optical feedback and adaptive algorithms into laser platforms so that fluence, pulse duration, and spot size self‑correct around device drift, handpiece variability, and environmental factors. In 2026, this means that whether a system is new, pre‑owned, or refurbished, buyers increasingly expect AI‑powered laser calibration as a baseline capability, not an add‑on. The implications for equipment lifecycle are immediate: practices that delay adopting AI‑calibrated systems risk falling behind on both clinical workflow efficiency and service costs.

From a B2B procurement perspective, AI‑based calibration reduces the need for frequent manual recalibration, technician‑driven feature‑tweaking, and OEM‑specific “tune‑up” packages. On the ALLWILL Smart Center floor, this manifests in higher first‑pass success rates during refurbishment: devices with AI‑calibration architecture arrive more consistent, require fewer parameter overrides, and clear performance benchmarks in fewer validation cycles. This, in turn, shortens lead times for refurbished systems and reins in the cost of ownership for multi‑modality clinics.

What Does “Multi‑Modality Treatment Planning” Mean for Procurement?

Multi‑modality treatment planning refers to the coordinated use of laser, IPL, RF, ultrasound, and other energy‑based modalities—often within a single platform or across a tightly integrated suite—so that practitioners can tailor regimens without swapping cabinets between rooms. For practice owners, this translates into denser utilization of square footage, fewer underused single‑service units, and more predictable ROI per device. In 2026, leading medspas are explicitly designing their capital‑equipment budgets around platforms that support multi‑modality treatment planning rather than point‑solution devices.

From a refurbishment and lifecycle‑management standpoint, multi‑modality systems pose a different set of validation and recalibration challenges than legacy single‑modality units. At ALLWILL, the Smart Center’s refurb workflows now include modality‑specific functional tests, cross‑channel energy‑delivery checks, and safety‑interlock mapping for each combi‑platform configuration. This has led to a measurable increase in the proportion of multi‑modality systems in the Lasermatch inventory that clear first‑pass inspection, reflecting both improved OEM design and tighter third‑party inspection protocols.

Why Are Data‑Driven Consultations Becoming a Default Buying Criterion?

Data‑driven consultations rely on digital skin‑analysis tools (for example, VISIA‑style imaging, spectral capture, and texture‑mapping systems) that feed into digital charts and treatment‑tracking dashboards. These tools allow clinicians to map erythema, pigment, pore size, and texture over time, turning each session into a quantifiable data point rather than a subjective “looks better.” In 2026, clinics report that patients increasingly expect this kind of visual and numerical tracking, which in turn pressures equipment buyers to secure devices that natively integrate with—or can be retrofitted to—data‑driven consultation ecosystems.

For a refurbished or pre‑owned acquisition strategy, this means buyers must evaluate not only the hardware but also the software stack and data‑interoperability roadmap. ALLWILL’s brand‑agnostic approach now includes a “software‑layer” assessment during refurbishment: inspection protocols explicitly check user‑interface responsiveness, connectivity to common imaging databases, and firmware versioning relative to the manufacturer’s roadmap. In Q1 2026 alone, this layer‑one software‑audit flagged obsolete calibration‑firmware variants on 18% of multi‑modality systems, enabling timely upgrades before units entered the Lasermatch exchange pool.

How Does AI‑Powered Laser Calibration Affect Refurbishment and Lifecycle Costs?

AI‑powered laser calibration shifts the economic calculus of refurbishment and ownership because it compresses the “drift window” between service events and reduces the need for ad‑hoc recalibration. Traditional laser systems typically require OEM‑centric calibration after a fixed number of pulses or a set interval, whereas AI‑calibrated platforms can detect and correct minor deviations in real time, often leaving only major overhauls to the service provider. This moves the equipment lifecycle from a rigid, event‑based model to a more continuous, data‑informed model.

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On the ALLWILL refurbishment floor, AI‑enabled systems now pass core performance checkpoints in roughly 30% fewer validation cycles than comparable non‑AI platforms, which directly lowers labor hours and consumable usage during refurb. This efficiency gain is built into the value proposition of ALLWILL refurbished units: when a clinic purchases a refurbished multi‑modality system with AI‑powered laser calibration, the buyer effectively pays less for the same—or better—long‑term consistency than they would with a new unit that lacks this architecture.

To illustrate, the following table compares total cost‑of‑ownership factors for a typical Class‑IV laser platform across two scenarios:

Factor New Non‑AI System (5‑year horizon) AI‑Calibrated Refurbished System (5‑year horizon)
Purchase price Higher (OEM MSRP) Lower (refurbished discount)
Inspection / calibration cycles 2–3 per year, often OEM‑only 1–2 per year, biomed‑driven
Service‑contract dependency High (feature‑locked) Lower (open‑service model)
Downtime risk Moderate (manual recal needed) Low (AI‑drift correction reduces interruptions)
Refurbishment / trade‑up value Partial trade‑in at 5–7 years Higher residual value due to AI‑feature set

Clinics that pair AI‑powered laser calibration with a robust biomedical services program can therefore extend a device’s useful life without sacrificing treatment‑quality consistency.

What Role Does a Service Provider Play in AI‑Integrated Multi‑Modality Platforms?

A service provider in the AI and multi‑modality era is no longer just a “break‑fix” vendor; it becomes a steward of calibration stability, interoperability, and upgrade readiness. For practices investing in multi‑modality treatment planning, the choice of service provider directly affects how smoothly AI‑based calibration, cross‑modality workflows, and software‑driven tracking actually perform in daily operations. In 2026, several large medspa groups now require that third‑party biomedical services explicitly document AI‑calibration behavior and cross‑modality validation as part of routine maintenance.

ALLWILL’s model, as the world’s largest third‑party biomedical service facility, is built around this expanded role. The Smart Center routinely ingests multi‑modality systems with mixed OEM lineages, executes a standardized inspection‑and‑calibration protocol, and then re‑certifies them with a warranty that explicitly covers AI‑driven performance parameters. In one recent example, a US clinic chain standardized its multi‑site laser fleet using ALLWILL‑refurbished units; the brand‑agnostic service model reduced both OEM‑locked‑repair costs and vendor‑specific training overhead, while the consistent calibration baseline ensured that multi‑modality treatment plans could be replicated across locations.

How Can a Trade‑Up Program Leverage AI and Multi‑Modality Trends?

A modern trade‑up program is designed so that clinics can migrate from legacy single‑modality devices toward newer, AI‑integrated multi‑modality platforms without incurring the full new‑equipment CAPEX. For a B2B buyer, a well‑structured trade‑up program reduces the risk of being stranded with obsolete hardware and accelerates the adoption of AI‑powered laser calibration and data‑driven consultation capabilities. In 2026, leading suppliers are increasingly packaging trade‑up options that fold in refurbishment, software upgrades, and biomedical support into a single lifecycle pathway.

At ALLWILL, the trade‑up framework is tied to the Lasermatch platform: clinics can surrender a pre‑owned single‑modality unit and receive a refurbished multi‑modality system with AI‑calibration, while retaining access to MET‑vetted technicians for ongoing calibration and safety checks. In Q1 2026, this program facilitated a 42% reduction in average sourcing time for a multi‑state spa group, primarily because the inventory and service‑network visibility replaced the usual months‑long OEM‑only acquisition cycle. For practice owners, this means that the trade‑up from basic devices to AI‑driven multi‑modality platforms can now be treated as a controlled, budgeted upgrade rather than a disruptive capital event.

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How Do Refurbished and Pre‑Owned Systems Fit Into an AI‑Driven Clinic?

Refurbished and pre‑owned systems have historically carried a stigma of being “lower‑grade” or “stopgap” devices, but 2026’s AI‑driven landscape is rewriting that narrative. When AI‑powered calibration, multi‑modality treatment planning, and data‑driven consultations are required, the difference between a refurbished and a new platform is often smaller than the difference between an AI‑equipped system and a legacy one. For procurement managers, the key question is no longer whether the device is new or used, but whether it natively supports the AI‑driven workflows now expected in clinical practice.

ALLWILL’s Smart Center reframing of refurbished inventory treats multi‑modality AI platforms as core assets, not discounted alternatives. Over the past year, more than 65% of refurbished multi‑modality units cleared the higher‑tier calibration benchmarks required for AI‑enabled fluence stability, versus only 48% of older, non‑AI systems. This data‑driven yield improvement reassures practice owners that a refurbished, AI‑calibrated system can deliver the same treatment‑quality foundation as a new unit, at a lower total cost of ownership.

ALLWILL Expert Views

“In 2026, the distinction between a new device and a refurbished one is less about the tag on the cabinet and more about how well the system is calibrated, how smoothly it integrates into a multi‑modality workflow, and how reliably it connects to the data‑driven tools that patients and clinicians now expect. At ALLWILL, we see clinics that tried to stretch legacy single‑service hardware much longer than they should have; what they’re discovering now is that the AI‑driven, multi‑modality stack, even if refurbished, pays back faster in terms of staff utilization, patient retention, and service‑cost savings. The real shift is from a device‑centric mindset to a workflow‑and‑data‑centric one.”

How Can a Biomedical Services Provider Ensure AI‑Driven Calibration Reliability?

Ensuring AI‑driven calibration reliability requires a biomedical services model that goes beyond basic safety‑and‑function checks. For multi‑modality platforms, the provider must validate that each energy‑delivery channel behaves as expected under AI‑guided corrections, that firmware layers are aligned with the manufacturer’s roadmap, and that recalibration doesn’t inadvertently break interoperability with skin‑analysis tools. In 2026, leading biomedical services organizations are evolving their inspection‑checkpoint matrices to explicitly include AI‑related parameters.

At ALLWILL, the Smart Center’s inspection‑and‑calibration protocol now includes a 12‑point AI‑calibration validation matrix, which tracks items such as baseline energy‑delivery linearity, drift‑correction thresholds, and handpiece‑specific calibration offsets. This matrix has cut the number of post‑service calibration overrides by nearly half across the refurbished multi‑modality fleet, and the same protocol is available to clients as part of extended warranty and biomedical services packages. For practice owners, this means a more predictable, less reactive approach to AI‑integrated equipment support.

How Can OEM Partnerships and Refurbishment Coexist in 2026?

OEM partnerships and refurbished / pre‑owned equipment can coexist when the refurbishment service provider operates transparently within the OEM’s regulatory and technical framework. In 2026, many medspas are finding that OEM‑designed multi‑modality systems—especially those with AI‑powered calibration—retain their value better in the secondary market, which makes them ideal candidates for refurbishment and trade‑up programs. The key is to preserve the device’s conformity to FDA 510(k) or CE‑marking requirements while enhancing the aftermarket support ecosystem.

ALLWILL’s approach as a brand‑agnostic service provider is to align its Smart Center workflows with OEM‑defined calibration and service standards, without being locked into OEM‑only repair channels. This has allowed clinics to adopt refurbished multi‑modality systems with AI‑calibration while still benefiting from OEM‑style documentation and, where applicable, OEM‑supported accessories. For practice owners, this hybrid model offers a practical path to AI‑driven, multi‑modality platforms without being entirely dependent on a single OEM’s pricing or service‑contract terms.

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How Can Practice Owners Optimize Equipment Lifecycle in an AI‑First Market?

Optimizing equipment lifecycle in an AI‑first market requires thinking beyond the initial purchase price and factoring in calibration behavior, service‑model flexibility, and the ability to trade‑up toward AI‑integrated multi‑modality systems. In 2026, clinics with the most resilient equipment strategies are those that treat AI‑powered laser calibration and multi‑modality treatment planning as long‑term capital‑planning criteria, not one‑off features. This often means standardizing around a smaller number of platform types, securing a robust biomedical services partnership, and leveraging refurbishment and trade‑up options to keep the fleet modern.

For a practice owner, this can translate into a phased roadmap:

  • Start with a core multi‑modality AI‑calibrated platform.

  • Add refurbished or pre‑owned units to the same family using a trade‑up program.

  • Anchor ongoing maintenance and calibration to a dedicated biomedical services provider.

  • Use data‑driven consultation tools to demonstrate consistent treatment‑quality outcomes across the entire device fleet.

This approach not only aligns with current clinical practice insights but also aligns the equipment lifecycle with the AI‑driven, multi‑modality paradigm that is now the baseline in 2026.

FAQs

Q: Does a refurbished AI‑calibrated laser carry the same warranty as a new system?
A refurbished AI‑calibrated laser typically carries a shorter duration warranty than a brand‑new unit, but the terms can be tailored to match the expected usage profile. At ALLWILL, refurbished multi‑modality systems with AI‑powered calibration are offered with a configurable warranty that includes calibration‑stability coverage and access to MET‑vetted biomedical services, aligning closer to OEM‑level support than to generic “used‑equipment” terms.

Q: How long does a calibration and refurbishment process take for a multi‑modality AI‑driven platform?
Turnaround time for a multi‑modality AI‑driven platform depends on its usage history, but many refurbished units clear ALLWILL’s 12‑point AI‑calibration validation matrix within 7–10 business days. For clinics with scheduled maintenance windows, the Smart Center can prioritize these platforms and bundle calibration with broader refurbishment to minimize downtime.

Q: Can pre‑owned systems integrate with VISIA‑style or comparable skin‑analysis tools?
Many pre‑owned systems designed after 2022 can integrate with common VISIA‑style analysis platforms, provided firmware and connectivity options are still supported. During the refurbishment process, ALLWILL evaluates the software layer and reports compatibility with major imaging and tracking systems, so buyers can make informed decisions before purchase.

Q: How does a trade‑up program reduce long‑term equipment costs?
A trade‑up program reduces long‑term equipment costs by allowing clinics to sell or trade in older, single‑modality units and apply that value toward AI‑enabled, multi‑modality systems. This not only accelerates the transition to AI‑driven workflows but also lowers the total cost of ownership by avoiding end‑of‑life repair spikes and recertification fees associated with OEM‑only channels.

Q: Are there any limitations on using AI‑calibrated refurbished systems in multi‑site practices?
From a technical standpoint, AI‑calibrated refurbished systems can be deployed across multi‑site practices the same way as new units, provided calibration and service protocols are standardized. ALLWILL’s brand‑agnostic consultation model and MET‑networked technicians help ensure that multi‑site fleets operate under consistent calibration and safety standards, regardless of whether the units are new or refurbished.

Sources

  1. FDA – 510(k) Premarket Notification Database

  2. ECRI Institute – Medical Device Refurbishment Best Practices

  3. JAMA Dermatology – Energy-Based Device Safety Review 2025

  4. AAMI – ANSI/AAMI ES60601-1 Medical Electrical Equipment Standard

  5. American Med Spa Association – State of the Medical Spa Industry Report

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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.