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ULTHERA DS 7-4.5 & DS 10-1.5N: Lower Face ROI & Price Guide

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For cervical and submental laxity, the ULTHERA DS 7-4.5 and DS 10-1.5N transducers work best as a paired protocol: 4.5 mm energy engages SMAS and platysma vectors in the lower face and neck, while 1.5 mm ultrasound polishes the dermis and subdermal plane along the jawline. This deep–shallow combination supports jawline contouring and neck crepiness work without promising specific outcomes, and can justify console and transducer investment when you model pricing, utilization, and sourcing across new and certified pre-owned units.

What These Transducers Do & Who They’re For

The ULTHERA DS 7-4.5 transducer is a DeepSEE cartridge designed to deliver microfocused ultrasound energy at approximately 4.5 mm focal depth, targeting the SMAS and fascia near the platysma in lower face and submental regions. It uses a 7 mm footprint to create lines of thermal coagulation in deep planes that support non-invasive vectoring along jawline and cervical contours.

The ULTHERA DS 10-1.5N is a 10 MHz, narrow-footprint transducer that treats at roughly 1.5 mm depth, engaging the dermis and very superficial subdermal tissues along small, curved fields such as the mandibular border, under-chin skin, and periorbital areas. Its role in lower face work is not fat removal but dermal quality and fine contour refinement in regions where skin is thinner and texture changes are easily perceived.

Clinics best suited to this combination are those offering Ultherapy Prime or similar advanced Ulthera protocols for jawline definition, double-chin contouring in mild-to-moderate laxity, and neck crepiness, especially where patients want non-surgical interventions. These are typically dermatology practices, medspas, and facial plastic surgery centers already comfortable with SMAS targeting and looking to refine their protocol architecture rather than adding another device category.

Technical Core: Jawline Vectors, Platysma Bands, and Deep–Shallow Layering

In lower face and neck work, jawline contour and cervical skin tone depend on three interacting elements: SMAS/platysma support, subcutaneous fat distribution, and dermal integrity. The DS 7-4.5 transducer focuses on SMAS and fascia near the platysma, generating thermal coagulation points that can influence mechanical support vectors along the mandibular border and under-chin region, while leaving superficial tissues largely intact.

The DS 10-1.5N transducer, by contrast, deposits energy within the dermis, stimulating collagen remodeling and localized tightening while affecting fine lines, texture, and crepiness rather than deep lift. Multiple clinical and practice-based sources describe using a combination of 1.5 mm, 3.0 mm, and 4.5 mm transducers to treat various layers of the face and neck, with the 4.5 mm cartridges focusing on SMAS and deeper lifting, and shallower cartridges focusing on dermal quality.

For jawline contouring and submental laxity, a typical mechanical rationale is:

  • Map vectors along the mandibular border and under-chin region based on anatomical lines of tension and platysma orientation.
  • Use DS 7-4.5 to create deep coagulation lines near SMAS/platysma, focusing on lower face and upper neck where laxity is most visible and bone must be avoided.
  • Follow, in selected cases, with DS 10-1.5N passes along the same or slightly offset vectors to compact the dermis and perceptually “sharpen” jawline and anterior neck texture, particularly for crepiness.

Microfocused ultrasound studies of the lower face show measurable changes in skin laxity and contour over several months, with protocols commonly using 3 mm and 4.5 mm depths; layered approaches aim to distribute energy across multiple planes for structural and textural effects. The Ulthera system’s imaging capability (DeepSEE) supports these protocols by allowing visualization of tissues up to about 8 mm below the surface, helping clinicians avoid bone and confirm proper coupling before delivering lines.

This mechanical understanding matters for procurement: you are not simply buying “double chin removal” devices, but a transducer pair that lets you construct and stabilize treatment vectors in deep and shallow planes, provided protocols stay within labeled indications and no specific clinical result is promised.

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Revenue and Payback Math for Lower Face Work

Ultherapy and similar HIFU/MMFU treatments for lower face and neck typically occupy high-fee slots in clinic menus, positioned as non-surgical contouring and tightening options for mild-to-moderate laxity. Incorporating both DS 7-4.5 and DS 10-1.5N into lower-face protocols can increase perceived sophistication and justify premium pricing, even though actual outcomes depend on patient selection and cannot be guaranteed.

Illustrative, non-binding economics for a mid-volume practice might look like:

  • Lower face and neck Ultherapy sessions priced around USD 1,500–2,500 per treatment, dependent on region and positioning.
  • 10–25 such sessions per month once the service is fully built out, with a significant subset using both DS 7-4.5 and DS 10-1.5N as part of multi-layer treatment mapping.
  • Incremental perceived value from dermal refinement (1.5 mm passes) helping clinics maintain prices towards the upper end of local ranges, though financial performance still depends on actual demand and retention.

On the cost side, the Ulthera console represents the largest fixed investment, with new DS 7-4.5 transducers often listed in the USD 3,000–4,500 range and DS 10-1.5N generally around USD 2,500–3,200 in primary markets, with variation by supplier and line-count package. Certified pre-owned transducers may be available at approximately 40–70% of new pricing, tied to remaining line counts, refurbishment scope, and warranty terms. (These ranges are estimates drawn from market listings; clinics must verify current figures.)

The payback model for lower face Ultherapy should incorporate:

  • Fixed capital: console plus an initial set of DS 7-4.5 and DS 10-1.5N transducers.
  • Variable cost: per-line usage across both depths, including eventual replacement and refurbishment.
  • Revenue: lower face/neck packages with clear internal protocols that utilize both depths to support vectoring narratives and justify tiered pricing.

ALLWILL can help clinic owners turn these data points into a true payback scenario, matching expected patient volumes and protocol mix with transducer inventory and lifespan rather than quoting hardware in isolation.

Request a quote from ALLWILL if you want DS 7-4.5 and DS 10-1.5N pricing presented alongside utilization, payback, and CPO condition modeling for your specific market.

Differentiated Advantage and High-Ticket Rationale

Many HIFU and MMFU platforms advertise lower face and neck tightening, but Ulthera’s combination of imaging and defined transducer architecture offers a more structured way to design protocols. The DS 7-4.5 transducer provides standardized SMAS targeting near platysma in lower face and submental regions, while DS 10-1.5N addresses superficial layers and texture, making them complementary tools for jawline and cervical work.

Clinical literature on microfocused ultrasound for lower face tightening highlights improvements in laxity and contour that develop over months, with protocols often using multiple depths to distribute thermal coagulation across different planes. Practice-based guides emphasize that a combination of 1.5 mm, 3.0 mm, and 4.5 mm transducers is commonly used in a single session to treat both SMAS and dermis. This multi-layer strategy differentiates Ultherapy-style approaches from devices that only offer a single focal depth or lack imaging for tissue visualization.

In procurement terms, the differentiated advantage is not just clinical but operational: Ulthera’s standardized cartridge ecosystem (including DS 7-4.5 and DS 10-1.5N), imaging, and treatment guidelines enable reproducible, protocol-driven lower-face work across clinicians and locations. Clinics can treat transducers as program components within a broader asset strategy, rather than ad-hoc accessories.

ALLWILL’s solutions positioning matches this reality by helping buyers think in terms of protocol architecture, transducer mix, and asset management instead of one-off hardware purchases.

Lower-Face Protocol Planning Framework (Jawline & Neck)

Because this topic centers on treatment planning rather than cost or logistics alone, the most useful decision aid is a tactical framework for designing lower-face protocols using DS 7-4.5 and DS 10-1.5N within realistic operational constraints.

Jawline & Cervical Ultherapy Protocol Planning Framework

  • Patient selection criteria
    • Focus on mild-to-moderate cervical and submental laxity with reasonably preserved volume; severe laxity or major submental fat may require other or combined approaches.
  • Anatomical mapping and vector design
    • Map jawline, under-chin, and anterior neck into zones based on platysma orientation, fat distribution, and skin thickness; define mechanical vectors that respect anatomical safety, avoiding bone and vital structures.
  • Device and transducer stack
  • Depth allocation strategy
    • Assign DS 7-4.5 passes to deeper SMAS/platysma zones in lower face and submental area; reserve DS 10-1.5N for superficial dermal refinement in jawline and crepey neck areas where texture and thin skin are prominent.
  • Energy and line-count planning
    • Estimate line numbers per zone and per depth based on manufacturer guidance and clinical best practices; align these with transducer line capacity and replacement timelines.
  • Coupling and imaging protocol
    • Standardize coupling gel type, thickness, and reapplication, and require DeepSEE imaging checks to confirm tissue planes and avoid bone before delivering lines.
  • Pricing and tiering structure
    • Design tiered lower-face/neck packages that clearly differentiate simple SMAS-focused treatments from multi-layer protocols, using internal language around layers and vectoring rather than outcome guarantees.
  • Follow-up and evaluation schedule
    • Set expectations for evaluation at three months and beyond, consistent with HIFU literature; incorporate standardized image-based assessments to track contour and laxity changes.
  • Asset tracking and maintenance
    • Integrate transducer usage logs, line-count tracking, and maintenance schedules into the clinic’s asset register; link DS 7-4.5 and DS 10-1.5N usage to specific protocols for better forecasting.
  • Training and SOPs
    • Develop written SOPs on jawline and neck mapping, depth selection, coupling, and safety checks; include Ulthera-specific steps and use these documents in onboarding and ongoing training.
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ALLWILL can help clinics formalize this framework into practical SOPs and asset plans, bundling transducer procurement with protocol design support, training recommendations, and maintenance scheduling.

Compliance and Asset Protection for Lower-Face Ultherapy

Ulthera-based Ultherapy systems hold FDA 510(k) clearance for specific non-invasive lifting indications such as brow, submental, and neck lifts and for improving the appearance of lines and wrinkles on the décolletage, with DeepSEE imaging supporting safe visualization of tissues. Clinics must verify the exact regulatory status of their console, transducer set, and any regional variations before deploying lower-face and neck protocols, especially cross-border.

Asset protection in this context means:

  • Verifying authenticity and traceability for each DS 7-4.5 and DS 10-1.5N transducer, including serial numbers, manufacturing dates, and sourcing channel.
  • Ensuring regulatory documentation and IFU materials for the Ulthera system are current and filed within the clinic’s compliance archive.
  • Obtaining written warranty terms for both console and transducers, including any specific line-count or time-based limitations.
  • For certified pre-owned units, requesting refurbishment reports, test results, and condition grading to understand exactly what has been done to each cartridge.

ALLWILL can facilitate verifiable, documentation-first sourcing by requiring such records from suppliers and organizing them for buyers, but clinics must still treat regulatory confirmation and asset tracking as internal responsibilities.

Request a quote from ALLWILL if you want lower-face Ultherapy hardware sourced with accompanying warranty, refurbishment, and regulatory documentation tailored to your jurisdiction and risk profile.

Procurement Risks to Avoid and ALLWILL Expert View

Key risks in procuring DS 7-4.5 and DS 10-1.5N transducers for lower-face work include buying from unverified channels, ignoring transducer condition and remaining line counts, and underestimating the importance of protocol alignment and training. Another risk is overselling “double chin removal” or jawline tightening as guaranteed outcomes, which can create misaligned expectations and regulatory exposure.

Clinics may also attempt to stretch transducers beyond recommended line usage to save cost, increasing variability in acoustic delivery and patient experience. Deploying refurbished units without clear test results and refurbishment documentation similarly introduces uncertainty into a high-visibility treatment zone.

ALLWILL Expert View: Building a Jawline & Neck Asset Strategy

From an asset perspective, lower-face Ultherapy is not just a console and a handful of cartridges; it is a protocol-driven service line anchored by specific depths and mechanical narratives. DS 7-4.5 and DS 10-1.5N have distinct roles in this architecture—deep SMAS/platysma vectoring and superficial dermal refinement—and your procurement plan should mirror that duality. Rather than ordering transducers opportunistically, we recommend mapping your jawline and cervical protocols first: define which depths you will use in each zone, how many lines per treatment, and what utilization you expect over a year. Only then do you specify how many new and CPO cartridges you need in rotation, with what line-count buffers.

ALLWILL’s experience is that clinics who treat lower-face Ultherapy transducers as coordinated assets—with line-count logs, refurbishment documentation, and maintenance schedules—see fewer surprises in uptime and patient experience. The quote process becomes a design step for your jawline and neck program, not just a price check. Structuring procurement this way protects your brand position in a competitive HIFU/MMFU market and keeps you within your risk and compliance tolerances without relying on any outcome guarantees.

If you are expanding into cervical and submental Ultherapy, ask ALLWILL for a transducer and protocol proposal that explicitly couples DS 7-4.5 and DS 10-1.5N with your intended jawline and neck treatment strategy.

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Frequently Asked Questions

What is the typical price range for DS 7-4.5 and DS 10-1.5N?

New DS 7-4.5 transducers frequently appear around USD 3,000–4,500, while DS 10-1.5N cartridges are often listed around USD 2,500–3,200 depending on supplier and line-count package. Certified pre-owned units can be lower, but exact pricing should be confirmed via a quote request.

How do new and certified pre-owned Ulthera transducers compare for lower-face work?

New cartridges offer full manufacturer warranty and predictable starting line counts, whereas certified pre-owned units can reduce capital outlay if refurbishment and testing are well documented. Clinics should compare remaining lines, membrane condition, and warranty terms in writing and can use ALLWILL to obtain structured CPO inspection summaries.

What regulatory considerations apply to jawline and neck Ultherapy?

Ulthera systems carry specific FDA 510(k) clearances and labeling for non-invasive lifting and related indications, but clinics must confirm that their particular console and transducer set are appropriately cleared or authorized in their region for intended use. Regulatory documentation should be reviewed and filed as part of procurement.

What ROI or payback timeline might I see for lower-face Ultherapy with dual depths?

ROI depends on session pricing, patient demand, and utilization across the lower face and neck menu. Many practices position dual-depth protocols to support premium tiers, but income is never guaranteed; a tailored payback model from ALLWILL can help estimate timelines under your local conditions.

What lead times and service requirements should I expect for these transducers?

Lead times for new DS 7-4.5 and DS 10-1.5N cartridges vary by region and stock, while certified pre-owned units may depend on refurbishment schedules. Buyers should clarify delivery timelines and service options in quotes and align them with maintenance plans to prevent treatment interruptions.

References

  1. Ulthera System – Instructions for Use (IFU)

  2. Ultherapy Prime Transducers: Depths and Their Specific Uses

  3. Introduction of the 1.5mm Shallow Transducer – Ulthera White Paper

  4. Evaluation of a Microfocused Ultrasound System for Improving Skin Laxity and Tightening in the Lower Face

  5. Three-dimensional Analysis of Lifting Effects after High-intensity Focused Ultrasound

  6. High-Intensity Focused Ultrasound (HIFU) for Facial Skin Tightening – Systematic Review

  7. Markham Ultherapy Prime – 7th-Generation Focused Ultrasound Overview

  8. ULTHERA_FT – Technical Overview of Ulthera System

  9. Ulthera DeepSee DS 10-1.5N Narrow Transducer – Listing and Specifications

  10. Ultherapy DeepSEE DS 7-4.5 (Purple) Transducer – Product Details

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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.