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Endymed Pro 3DEEP: What Clinic Owners Must Know Before Buying

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The Endymed Pro 3DEEP is an FDA-cleared, multi-application RF microneedling and fractional resurfacing platform used for non-surgical skin tightening, acne scar revision, and body contouring. New units typically list between $45,000–$75,000 depending on configuration and region, while certified pre-owned (CPO) systems in verified condition commonly trade in the $18,000–$35,000 range. Payback for most clinics occurs within 6–14 months when pricing treatments at $800–$1,500 per session and running 10–20 procedures monthly.

What is the Endymed Pro 3DEEP and which treatments does it support?

The Endymed Pro 3DEEP is an all-in-one RF platform combining fractional microneedling (Intensif), fractional skin resurfacing (FSR), and non-ablative deep heating (Deep) for face and body indications. It is FDA-cleared for improving facial acne scars, wrinkles, and abdominal scars in patients 22+, and is used off-label for pores, stretch marks, and mild skin laxity.

The system’s core is EndyMed’s proprietary 3DEEP multi-source, phase-controlled RF technology, which delivers energy in a controlled, phased sequence across multiple electrodes. This creates uniform dermal heating to approximately 52–55°C while minimizing epidermal temperature rise — a key factor in patient comfort and safety.

Clinically, the platform supports:

  • RF Microneedling (Intensif handpiece): Adjustable needle depth from 0.5–5.0 mm in 0.1 mm increments; pulse duration 50–200 ms; energy 0–25 W (±20%). Indications include acne scars, deep wrinkles, enlarged pores, and textural irregularities.
  • Fractional Skin Resurfacing (FSR handpiece): Non-ablative fractional RF for superficial resurfacing, fine lines, and mild dyschromia. Often combined with microneedling in a “3DEEP Trio” protocol.
  • Deep RF handpiece: Non-invasive deep dermal heating for body contouring, skin tightening on abdomen, thighs, arms, and buttocks. Penetration up to 9 mm depending on technique and settings.

The device is positioned as a physician-grade tool with granular control over depth, energy, and pulse width, enabling customization across Fitzpatrick skin types when protocols are followed.

How do hardware physics and calibration affect uptime and safety?

RF microneedling safety hinges on real-time impedance monitoring and a tightly calibrated feedback loop between the handpiece, controller, and tissue. Impedance — the tissue’s resistance to current flow — varies by hydration, thickness, and temperature. If the system cannot read and react to impedance changes within milliseconds, energy delivery becomes unpredictable, increasing burn and arcing risk.

On the Endymed Pro, the dynamic impedance feedback loop is designed to adjust power output in under 10 ms when functioning to factory spec. This rapid response prevents localized overheating as needles penetrate and tissue resistance shifts. Clinical engineers emphasize that calibration drift — common in older or poorly maintained secondary-market units — can introduce latency or sensor error, effectively “blinding” the device to real tissue conditions.

Key hardware factors that influence reliability:

  • Impedance sensor accuracy: Factory calibration ensures the sensor reads tissue resistance within a narrow tolerance. Out-of-calibration sensors may under- or overestimate impedance, leading to excessive energy or premature cutoffs.
  • Controller-board firmware and timing: The PLC and RF power module must synchronize pulse timing and phase control precisely. Firmware mismatches or degraded components can create microsecond-level delays that compound into unsafe energy profiles.
  • Handpiece integrity: Intensif tips contain micro-needle arrays and RF pathways that degrade with cycles. Bent pins, oxidized contacts, or micro-fractures in the insulator can cause arcing or uneven energy distribution.
  • Preventive maintenance (PM) cadence: Regular electrical safety testing, calibration verification, and handpiece cycle tracking are essential. Typical PM intervals are 6–12 months depending on usage intensity and local regulations.

For clinic owners, this means condition grading and documentation matter more than brand name when buying used. A CPO unit with a full refurbishment report, calibration certificate, and PM history is often a safer long-term asset than a “patient-ready” unit with no service records.

Why does total cost of ownership matter more than sticker price?

The purchase price of an Endymed Pro is only one component of total cost of ownership (TCO). Clinics that ignore consumables, financing, maintenance, and downtime often underestimate the true cost by 20–40% over a 3–5 year horizon.

Major TCO drivers include:

  • Device acquisition cost: New vs CPO vs used “as-is.” New units carry full OEM warranty but higher upfront cost. CPO units from reputable refurbishers offer mid-range pricing with limited warranty and documented service history. Untested used units may be cheapest initially but carry the highest risk of early failure and unplanned expense.
  • Financing and lease terms: Equipment finance agreements (EFAs), $1 buyout leases, and deferred-payment options are common in aesthetics. Monthly payments for a $50,000 device typically range from $800–$1,500 depending on term, interest, and buyout structure.
  • Consumables and disposables: Intensif treatment tips are single-use or limited-reuse depending on local regulation and manufacturer guidance. Pricing per tip commonly falls in the $80–$150 range, with volume discounts for larger practices. FSR and Deep handpieces may have lower per-treatment consumable costs but still require periodic replacement parts.
  • Maintenance and calibration: Annual service contracts or per-visit calibration can run $1,500–$4,000 depending on provider and scope. Unexpected repairs (controller board, handpiece replacement) can add $3,000–$10,000+ if not covered by warranty.
  • Downtime cost: Every day the device is out of service represents lost revenue. A clinic running 15 RF microneedling treatments per week at $1,000 average could lose $6,000+ monthly during extended downtime.
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Smart buyers model TCO explicitly: acquisition + financing + consumables + service – residual value over their intended hold period. This often reveals that a slightly higher-priced CPO unit with warranty and documented service is more economical than a bargain “as-is” unit with unknown history.

How does the Endymed Pro compare clinically to other RF microneedling platforms?

Buyers frequently compare the Endymed Pro 3DEEP to systems like Morpheus8, Profhilo-based protocols, and other RF microneedling devices. The differences lie in needle design, energy delivery, depth control, and treatment versatility rather than any single “best” technology.

Feature Endymed Pro 3DEEP (Intensif) Morpheus8 (InMode) Typical Generic RF Microneedling
Needle type Non-insulated gold-plated needles Insulated needles Varies (often non-insulated)
Energy delivery RF along entire needle length RF primarily at needle tip RF along needle or tip-dependent
Depth range 0.5–5.0 mm, adjustable in 0.1 mm steps Typically up to 4–8 mm depending on handpiece Often 0.5–3.5 mm
Applications Acne scars, wrinkles, pores, body tightening Deep tightening, contouring, scars Primarily facial rejuvenation
Platform flexibility Multi-handpiece (Intensif, FSR, Deep) Multiple handpieces but often separate platforms Often single-function
Comfort features 3DEEP phased RF, controlled dermal heating Fractional bipolar RF, variable pulse Variable, often less controlled

Non-insulated needles (Endymed) deliver energy along the full tract, favoring comprehensive dermal remodeling and superficial-to-mid dermis treatment — advantageous for pores, texture, and rosacea-related concerns. Insulated needles (Morpheus8) concentrate energy at the tip, favoring deeper, more focal heating with less epidermal impact — useful for deep laxity and contouring.

Clinics that prioritize versatility across face and body may value the Endymed Pro’s multi-handpiece architecture and ability to run combined protocols (e.g., microneedling + FSR + Deep in one session). Practices focused primarily on deep subdermal tightening or body contouring may lean toward platforms optimized for those indications.

Which ROI and procurement framework should guide a high-ticket device decision?

For a capital purchase in the $20,000–$75,000 range, clinics benefit from a structured decision framework that balances clinical fit, financials, compliance, and supplier risk. The following BME Technical & Procurement Decision Matrix is designed for clinic owners, operators, and biomedical engineers evaluating an Endymed Pro or similar RF microneedling platform.

BME Technical & Procurement Decision Matrix

Use this as a checklist and scoring tool. Rate each item 1–5 (1 = poor/unknown, 5 = excellent/fully documented).

1. Clinical Fit & Indications

  • Does the device’s cleared indications match your target patient profile (acne scars, wrinkles, body tightening)?
  • Can your providers be trained to use adjustable depth and energy safely across skin types?
  • Is there evidence of demand in your market for RF microneedling at your planned price point?

2. Hardware Condition & Uptime Risk

  • Is there a full refurbishment report with calibration certificate and PM history?
  • Are handpiece cycle counts known and within recommended limits?
  • Has electrical safety testing (leakage, ground resistance) been performed within the last 12 months?
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3. Total Cost of Ownership (3–5 Year Model)

  • Have you modeled acquisition + financing + consumables + service – residual value?
  • Are consumable costs per treatment realistic for your projected volume?
  • Is there a clear service plan and estimated annual maintenance budget?

4. Compliance & Regulatory Status

  • Is the device’s FDA 510(k) or CE status current and applicable to your region and intended use?
  • Does the seller provide documentation of regulatory compliance and import eligibility (if cross-border)?
  • Are software versions supported and upgradable to current standards?

5. Supplier Trust & Asset Protection

  • Does the supplier offer transparent condition grading (new, CPO, refurbished, used) with clear definitions?
  • Is there a written warranty covering parts, labor, and handpiece functionality? For how long?
  • Can the supplier provide references, inspection reports, and post-sale support (training, troubleshooting)?

Score each section and look for patterns: a high clinical fit score with low hardware or supplier scores signals elevated risk. ALLWILL’s approach is to align clinics with vetted, compliance-aware suppliers and CPO units that include calibration logs, PM records, and clear warranty terms — reducing the likelihood of costly surprises post-purchase.

ALLWILL Expert View
From a procurement and asset-protection standpoint, the single biggest mistake we see clinic owners make is optimizing for lowest upfront price while ignoring calibration history and service documentation. On RF microneedling platforms like the Endymed Pro, a unit that has been properly refurbished, calibrated, and electrically tested — even at a 10–15% premium — almost always delivers lower total cost of ownership over 3–5 years. The hidden costs of unplanned downtime, emergency repairs, and compromised patient safety far outweigh the initial savings. When sourcing through ALLWILL, we insist on seeing full refurbishment reports, calibration certificates, and PM histories before matching a clinic with a CPO unit. Our role isn’t to push inventory; it’s to ensure the device you buy becomes a revenue-generating asset, not a liability.

What compliance and asset-protection steps protect clinics post-purchase?

Once a device is acquired, ongoing compliance and asset protection are critical to maintaining safety, regulatory standing, and resale value. This is especially true for energy-based devices with moving parts, high-voltage components, and disposable handpieces.

Key post-purchase practices include:

  • Preventive maintenance schedule: Adhere to manufacturer-recommended PM intervals (typically 6–12 months). Document all service, calibration, and electrical safety tests in a central equipment log.
  • Handpiece cycle tracking: Record the number of pulses or treatments per Intensif tip and other handpieces. Replace tips at or before the recommended cycle limit to avoid performance degradation and safety risks.
  • Staff training and protocol standardization: Ensure all operators are trained on device settings, impedance monitoring cues, and emergency shutoff procedures. Standardized protocols reduce variability and adverse event risk.
  • Regulatory documentation: Maintain copies of FDA 510(k) summaries, CE certificates (if applicable), and import documentation. Update these records if software or hardware upgrades change the device’s regulatory status.
  • Incident logging and risk management: Log any adverse events, near-misses, or device malfunctions. Use this data to refine protocols and, if necessary, engage the supplier or service provider for root-cause analysis.

For clinics considering future upgrades or trade-ins, well-documented maintenance and compliance records significantly enhance resale or trade-in value. ALLWILL’s two-way equipment trade-in program, for example, factors in condition grading, service history, and regulatory documentation when evaluating a device for credit toward a new or CPO system.

Which procurement risks should clinic owners actively avoid?

Several recurring pitfalls can turn a promising device purchase into a costly, compliance-heavy headache. Awareness and due diligence are the best defenses.

Common risks include:

  • Buying “as-is” with no service history: Units sold without calibration logs, PM records, or electrical safety tests carry a high risk of latent defects. These often surface as intermittent faults, sensor errors, or handpiece failures within months.
  • Ignoring regional regulatory requirements: A device cleared in one jurisdiction may not be compliant in another. Importing without verifying FDA, CE, or local health authority requirements can lead to customs delays, fines, or inability to use the device legally.
  • Overlooking consumable and handpiece costs: Some platforms appear affordable upfront but have expensive or short-life disposables. Failing to factor these into TCO can erode margins quickly.
  • Relying on verbal warranties or vague promises: Always secure written warranty terms covering parts, labor, handpiece functionality, and response times. Verbal assurances are difficult to enforce and often exclude critical components.
  • Underestimating training and protocol development: Even experienced providers need device-specific training to leverage advanced features like adjustable depth, impedance monitoring, and multi-handpiece protocols. Skipping this step increases adverse event risk and underutilization.
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For clinics seeking a lower-risk path to acquiring an Endymed Pro or similar platform, engaging a compliance-aware sourcing partner can mitigate many of these risks. ALLWILL’s model emphasizes vetted suppliers, transparent condition reports, and post-sale support to ensure clinics receive devices that are not only functional but also compliant and economically viable over the long term.

If you’re evaluating an Endymed Pro 3DEEP and want current pricing, availability, and condition reports on certified pre-owned units, request a quote from ALLWILL. Their team can provide detailed refurbishment documentation, warranty terms, and financing options tailored to your clinic’s cash flow and growth plans.

Frequently Asked Questions

What is the typical price range for a new vs certified pre-owned Endymed Pro 3DEEP?
New Endymed Pro systems typically list between $45,000–$75,000 depending on configuration and region. Certified pre-owned (CPO) units in verified condition with documented refurbishment and calibration history commonly trade in the $18,000–$35,000 range. The wide variation depends on included handpieces, tip inventory, age, and warranty coverage.

Is the Endymed Pro 3DEEP safe for all skin types (including darker skin tones)?
Yes, when used with correct protocols. The 3DEEP multi-source phase-controlled RF technology provides controlled dermal heating with minimal epidermal temperature rise, which reduces the risk of hyperpigmentation or burns in Fitzpatrick skin types IV–VI. However, proper training on adjustable depth and energy settings is essential, and a patch test is recommended for higher-risk patients.

How much do the consumables (Intensif tips) cost per treatment, and how many uses do they last?
Intensif single-use or limited-use tips typically cost between $80–$150 per tip, depending on volume discounts. While manufacturer guidance generally recommends single-use to ensure sterility and optimal RF performance, some clinics in certain regions may use limited-reuse protocols. For accurate per-treatment consumable cost modeling, you should factor in 1–2 tips per full-face procedure, plus occasional replacement costs for FSR and Deep handpiece components.

How does the Endymed Pro 3DEEP compare to Morpheus8 in terms of clinical outcomes and patient comfort?
The main difference lies in needle design: Endymed uses non-insulated gold-plated needles that deliver RF energy along the entire needle tract, favoring comprehensive superficial-to-mid dermal remodeling (better for pores, texture, and rosacea). Morpheus8 uses insulated needles that concentrate energy at the tip for deeper focal heating (better for deep laxity and contouring). For comfort, Endymed’s 3DEEP phased RF technology provides more controlled dermal heating with less epidermal discomfort, but actual patient experience depends on settings, technique, and topical anesthesia.

What are the most common hidden costs when buying a used Endymed Pro on the secondary market?
The most common hidden costs include: (a) calibration drift requiring immediate re-calibration ($1,500–$4,000), (b) degraded handpiece components or connectors that need replacement ($3,000–$10,000+), (c) missing or outdated firmware that affects performance and safety, (d) lack of service history leading to unplanned downtime (potentially $6,000+ per month in lost revenue), and (e) non-transferable or expired warranties that leave you exposed to full repair costs.

What is the typical useful lifespan of an Endymed Pro 3DEEP platform with proper maintenance?
With regular preventive maintenance (every 6–12 months), calibration verification, and proper handpiece cycle tracking, the main console and controller board typically remain clinically viable for 7–10+ years. Handpieces and consumable tips are shorter-lived (tips are single-use or limited-use; FSR and Deep handpieces may need replacement every 2–5 years depending on usage). Well-documented service records also significantly enhance resale or trade-in value when you eventually upgrade.

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        7.  CANCELLATION CHARGES AND RETURNED EQUIPMENT POLICY. Returns and cancellations are not permitted without written approval by an MRP Officer, which shall be made in such MRP Officer’s sole discretion. If approved, MRP will issue a return merchandise authorization number, which Buyer must include in the returned packaging, and Buyer must pay MRP either a (a) twenty percent (20%) restocking charge on the purchase price of the item if Buyer’s written request for return or cancellation is received by MRP’s headquarters after MRP’s original shipment of the Equipment or (b) a ten percent (10%) cancellation damages charge if Buyer’s request was received before said shipment. The foregoing charges are agreed upon, not as a penalty, but because of the difficulty of computing actual damages, and until the applicable charge is paid and the Equipment has been received back by MRP in new condition, no refund will be given. This document or copies hereof may be filed with the appropriate authorities as a financing statement to pursue such charges. In no case will shipping and freight costs be refunded. Removed, replaced or substituted equipment and parts (collectively, “Returned Equipment”) shall become MRP’s property, with title and ownership transferring to MRP upon the earlier of its return or replacement, with MRP owing no other obligations on the Returned Equipment. Buyer hereby agrees to indemnify, defend and hold harmless MRP Indemnitees from any claims, costs, losses, attorneys’ fees and expenses related to any third-party attempts to claim ownership of the Returned Equipment or dispute any trade-in, removal, substitution or replacement, and the remaining provisions shall continue in full force and effect.

        8.  MRP’S WARRANTIES, IF ANY.

(a) Equipment Sold “As Is.” UNLESS OTHERWISE STATED ON THE QUOTE OR IN A WRITING SIGNED BY AN MRP OFFICER, BUYER AGREES THAT THE EQUIPMENT SOLD IN THIS AGREEMENT IS BEING SOLD ON AN “AS IS,” “AS AVAILABLE” BASIS, SUBJECT TO SECTIONS 8(c) AND 9, AND HAVE NO WARRANTIES OR REPRESENTATIONS OF ANY KIND, WHETHER IMPLIED OR ARISING BY LAW, STATUTE OR OTHERWISE, INCLUDING, WITHOUT LIMITATION, ANY WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE OR USE, NON-INFRINGEMENT, WORKMANLIKE MANNER, QUALITY, ACCURACY, TITLE, AND/OR IMPLIED FROM A COURSE OF DEALING OR PERFORMANCE USAGE IN TRADE.

(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.

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(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.