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800-Line Ultherapy & HIFU Face–Neck Master Protocols: Cost, ROI & Training Guide

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For a clinic planning full-face and neck tightening with advanced 800-line Ultherapy or HIFU schemes, expect a capital device budget in the low six figures (new) or high five figures (certified pre-owned), plus per-case consumable and staff-training costs that typically allow treatment margins of 60–75% depending on pricing and utilization. When planned at tri-depth intersections with all three probes, most clinics see payback in 12–24 months if treatments are correctly priced, marketed, and clinically standardized.

What these protocols do & who they fit

High-intensity focused ultrasound (HIFU) and microfocused ultrasound with visualization (MFU-V, used in Ultherapy) deliver thermal coagulation points at precise depths to trigger neocollagenesis and tissue contraction in the dermis, deep dermis, and SMAS layer without incisions. Tri-depth, full-face and neck protocols use multiple probes (for example, around 1.5 mm, 3.0 mm, and 4.5 mm) to address superficial texture, mid-dermal support, and deeper fascial tightening in a single comprehensive session.

The 800-line Ultherapy guidelines and similar HIFU schemes represent an advanced energy-delivery plan that increases total shots and energy distribution versus older 500–600 line standards, often used for moderate laxity and more visible lifting objectives. These protocols best fit clinics and medspas positioning themselves as premium non-surgical lifting centers, where patients accept higher ticket pricing in exchange for doctor-guided assessment, ultrasound visualization, and comprehensive face–neck coverage.

Topic-specific core analysis: advanced 800-line tri-depth training focus

Because your working title centers on “Advanced 800-Line Masterclass Protocols” and “advanced aesthetic practitioner training,” the most valuable focus is systematic protocol design and staff upskilling rather than generic device specs or price-only talk. The aim is to standardize full-face and neck Ultherapy/HIFU lines into a repeatable, tri-depth scheme that your team can deliver consistently while staying within manufacturer safety parameters and patient-tolerance thresholds.

In practice, full-face and neck MFU-V protocols often range from roughly 800 lines for comprehensive face coverage to 1,200–1,400 lines when neck and additional areas are included, with line counts allocated to upper face, midface, jawline, submental region, and neck based on tissue laxity and bone/nerve landmarks. A masterclass-level implementation teaches practitioners how to translate these ranges into individualized maps: marking orbital margins, mandibular curves, cheek planes, and nerve-sparing zones, then stacking probe passes at different depths with slight line overlap to build a three-dimensional grid of thermal points.

Training must go far beyond “how to fire lines” and cover visualization interpretation (where available), energy titration, patient communication, analgesia planning, and post-treatment expectations to avoid under-treatment or over-treatment at critical intersections like the jawline and anterior neck. ALLWILL can support this by matching clinics with experienced MFU-V and HIFU trainers, providing protocol templates, and coordinating remote or on-site sessions tailored to your device mix and regulatory environment.

Request a quote from ALLWILL for device options, training support, and an 800-line protocol planning session customized to your clinic’s case mix.

Revenue and operational impact & payback math

From a business perspective, full-face and neck Ultherapy or advanced HIFU lifting sits firmly in the high-ticket category, with patient fees in many markets falling roughly into the mid-to-high four-figure range per comprehensive session, depending on brand positioning and region. Because protocols like 800–1,200 lines are usually delivered as single, intensive treatments, they lend themselves to clear package pricing and add-ons (for example, brow-only, lower face-only, or neck-focused mini schemes) that can broaden your offer stack without fully replicating the master protocol each time.

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On the cost side, Ultherapy and similar MFU-V systems typically require an upfront capital investment that may sit around low-to-mid six figures new and somewhat lower for certified pre-owned, while generic HIFU platforms trend lower but still represent meaningful capital decisions. Assuming a per-treatment internal cost that includes device amortization, staff time, analgesia, gel, and maintenance allocations, many clinics see gross margins of 60–75% per mastersession when utilization is adequate and no heavy discounts are applied.

Illustratively, a clinic performing 15–25 full-face and neck 800-line sessions per month at a solid market price point can often reach payback in roughly 12–24 months, provided that marketing, consultation conversion, and patient satisfaction are managed effectively. ALLWILL’s Smart Center and advisory services can help model these numbers for your local pricing and capacity, and evaluate whether a new or certified pre-owned unit better aligns with your cash flow and utilization forecasts.

Differentiated advantage and higher-ticket rationale

Advanced tri-depth Ultherapy and HIFU master protocols distinguish your clinic not because they promise guaranteed outcomes but because they signal depth of planning, safety-aware line distribution, and adherence to evidence-based guidelines. MFU-V systems like Ultherapy incorporate real-time visualization to confirm tissue depth, allowing more confident placement of thermal coagulation points relative to bone, vessels, and nerves, which many physicians view as an important differentiator in premium non-surgical lifting.

Compared with more generalized HIFU platforms, brand-recognized MFU-V devices may also carry established FDA clearance or CE marking for specific facial and neck indications, which some patient segments look for when choosing higher-price non-surgical lift options. Devices like Ultherapy are frequently considered alongside other non-surgical lifting systems such as HIFU-based platforms and radiofrequency microneedling solutions; each has different cost, comfort, and downtime profiles that your practitioners should be able to explain neutrally.

For clinic owners, the real differentiator is not just the logo on the console but the presence of standardized mapping, tri-depth logic, and staff training that make 800-line and above schemes repeatable with careful patient selection and realistic expectation setting. ALLWILL’s positioning as “We Don’t Sell, We Solve” is specifically aligned with helping you select hardware, probes, and training pathways that fit your intended tier of service rather than pushing a single brand.

Practical B2B decision aid: Advanced tri-depth protocol & training framework

For this topic, a tactical framework is more useful than a cost table. Use the following as a starting point for designing your 800-line full-face and neck program and staff masterclass.

Advanced 800-Line Face & Neck Tri-Depth Training Framework

  1. Protocol definition
    • Decide your standard full-face and neck line range (for example, 800–1,200 lines for moderate laxity) while staying within device and manufacturer guidance for energy and total shots.
    • Define variations for partial protocols: upper face–brow, midface–jawline, neck-only.
  2. Tri-depth probe mapping
    • Assign superficial probe passes to fine lines and surface texture planes, mid-depth passes to cheek and jawline support, and deep passes to SMAS and submental lift targets.
    • Standardize approximate line allocations per depth and region (for example, percentages rather than fixed counts) to allow for individualized adjustments.
  3. Anatomical landmark & safety training
    • Train staff to mark infraorbital margins, mandibular curves, cheek planes, and nerve-sparing zones using rulers and planning markers.
    • Include case-based drills where operators adjust line density around high-risk structures while maintaining coverage.
  4. Visualization and energy titration
    • For MFU-V systems, incorporate ultrasound image interpretation into training, emphasizing how to confirm target depth before firing.
    • Define energy ranges per probe and region, plus protocols for incremental energy adjustments based on patient tolerance.
  5. Patient pathway and expectations
    • Build consultation scripts that clearly explain non-surgical lifting mechanisms, number of lines, and realistic timelines for visible changes without promising specific outcomes.
    • Train staff to document baseline photos and standardized follow-up intervals to support clinical audits.
  6. Quality assurance and audit cycle
    • Implement periodic case reviews to ensure line counts, mapping, and depth settings match your agreed protocol ranges and manufacturer guidance.
    • Use device logs and treatment records to monitor consistency and identify any drift from standard parameters.
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ALLWILL can help refine this framework for your device brand, regulatory environment, and staffing model, and connect you with experienced trainers who already work with Ultherapy and similar platforms.

Request a quote from ALLWILL to review suitable devices, map your tri-depth protocol framework, and schedule advanced practitioner training for your team.

Compliance and asset protection

Ultherapy is cleared by the US FDA for non-invasive lifting of the skin on the face, neck, and brow, as well as for specific décolletage indications, and similar MFU-V/HIFU systems may hold CE marking or other regional approvals for defined aesthetic uses. That said, regulatory status varies by country and can change, so it is essential that clinic owners verify current clearance or certification for their device model and intended indications directly with manufacturers or regulatory databases before launching or marketing treatment programs.

Safety and asset protection depend not only on hardware but on diligent adherence to manufacturer protocols, periodic servicing, and operator competence. Certified pre-owned units should come with verifiable service histories, calibration records, and proof of authenticity, and they should be inspected and refurbished according to manufacturer-equivalent or clearly stated third-party standards rather than assumed to be identical to new devices.

From a contractual standpoint, clinics should insist on written documentation covering device origin, serial numbers, probe compatibility, warranty terms, and any training obligations or support provisions attached to the purchase. ALLWILL’s sourcing and Smart Center services are designed to facilitate this verification process, but clinic owners should still treat themselves as the final compliance gatekeepers, especially for YMYL technologies that influence both patient safety and financial risk.

Procurement risks to avoid + ALLWILL Expert View

Common procurement risks with high-ticket MFU-V and HIFU systems include underestimating total cost of ownership, overlooking probe and consumable lifecycles, and buying hardware without a clear plan for staff training and protocol standardization. Another frequent issue is assuming that any “HIFU” branding equates to the same regulatory profile as MFU-V devices like Ultherapy, which is often not the case; regulatory indications must be checked per model, not per marketing term.

Clinics also risk operational disruption when acquiring devices without confirmed local servicing and parts availability, leading to downtime and cancelled sessions if a transducer or key component fails. ALLWILL mitigates these risks by vetting suppliers, clarifying service pathways, and providing condition reports for certified pre-owned units, but owners should still schedule periodic protocol audits and business reviews to ensure the device continues to align with patient demand and financial performance.

ALLWILL Expert View: Turning 800-Line Protocols into a Bankable Asset

When clinic owners look at tri-depth 800-line face–neck protocols, they often focus first on hardware price and energy-line counts. From an asset-management viewpoint, the priority should be mapping those lines to utilization, patient mix, and operator skill. A high-spec MFU-V system with poorly trained staff and inconsistent mapping will underperform financially even if the technology is sound. Conversely, a certified pre-owned unit deployed with rigorous training, documented protocols, and realistic pricing can become a stable revenue engine with lower capital outlay. The most resilient clinics treat these devices as managed assets: they model payback based on conservative monthly case volumes, protect uptime through verified servicing, and tie every protocol update to both clinical audit data and margin tracking. In this approach, ALLWILL’s role is to help you acquire a device whose cost structure, service history, and training ecosystem support that asset strategy, rather than simply adding another console to your treatment room.

To evaluate new vs certified pre-owned options under this asset-focused lens, request a quote from ALLWILL for current pricing, condition reports, and training packages matched to your team’s experience level.

Frequently Asked Questions

What is the typical price range for full-face and neck Ultherapy or advanced HIFU treatments?

In many markets, comprehensive full-face and neck MFU-V or HIFU lifting sessions are priced in approximately the mid-to-high four-figure range, with variations based on brand, practitioner credentials, and region. These figures are illustrative only; clinics should benchmark local competitors and cost structures, then adjust pricing accordingly and consider requesting a quote from ALLWILL for device-level cost inputs.

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How do new and certified pre-owned devices differ in cost and risk?

New MFU-V systems generally command low-to-mid six-figure investments, whereas certified pre-owned units may sit in the high five-figure band depending on age, condition, and brand. CPO devices can reduce capital outlay but require careful verification of service history, calibration, probe compatibility, and warranty, all ideally documented in writing.

What kind of warranty and support should I expect?

Warranty terms vary widely by manufacturer and reseller, typically covering major components for a defined period with optional extensions. Clinics should clarify coverage for consoles, transducers, software, and training, and confirm how service is delivered (on-site vs depot) before committing; ALLWILL can help outline realistic support options during the quote process.

How do regulatory and import factors affect procurement?

MFU-V and HIFU devices may hold FDA clearance, CE marking, or other regional approvals for specific indications, but import rules and registration requirements differ by country. Buyers must verify that their selected unit and model meet local regulatory standards and that all customs and documentation steps are properly handled to avoid delays or compliance issues.

What is a reasonable payback period for an 800-line protocol program?

For clinics with steady demand and effective marketing, a payback period in the 12–24 month range is common for high-ticket MFU-V/HIFU systems, assuming consistent monthly case volume and robust pricing. This is not a guarantee; each clinic should model its own numbers, but a tailored quote and ROI discussion with ALLWILL can help ground your expectations.

References

  1. Ultherapy PRIME in Singapore | Non-Surgical Skin Lifting Treatment
  2. Get to Know: Ultherapy, the Skin-Tightening Treatment for a Youthful Appearance
  3. Hi5 Protocol for the Use of Microfocused Ultrasound with Visualization
  4. Ultherapy SPT Program: Deep Skin Tightening Without Surgery
  5. Ultherapy Facial Treatment Guidelines – PrettyLasers
  6. Ulthera Amplify with New 800 Line Guideline – Dr. Michael Persky
  7. Ultherapy Treatment: How Many Shots Needed? – Visodent NY
  8. Ultherapy Seoul 2026: Prices, Lines & More – Korea Derma Guide
  9. ALLWILL | B2B Medical Aesthetic Devices & Solutions
  10. Certified Provider Platform – Sundrata Clinic
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        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.