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Is SYLFIRMX RF Microneedling Worth It for Skin Rejuvenation?

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RF microneedling has become one of the fastest‑growing modalities in medical aesthetics, with SYLFIRMX emerging as a leading dual‑wave platform for non‑surgical skin tightening, texture refinement, and vascular‑related pigmentation. For clinics and medspas, investing in a proven, versatile device like SYLFIRMX can translate into higher patient satisfaction, repeat bookings, and stronger differentiation from injectable‑only practices. When paired with a reliable B2B partner such as ALLWILL, practices can reduce capital risk while still offering premium‑tier treatments.

Why Is the RF Microneedling Market Growing So Fast?

The global radiofrequency microneedling market is projected to expand by more than 10% annually over the next several years, driven by rising demand for minimally invasive skin tightening and scar‑remodeling solutions. Aesthetic clinics report that RF microneedling now accounts for roughly 15–20% of non‑surgical facial procedures, with SYLFIRMX‑style dual‑wave systems frequently cited as preferred devices for both anti‑aging and vascular‑pigment indications. This growth reflects a broader shift: patients increasingly expect visible, long‑lasting results without extended downtime or surgical risk.

Despite this momentum, many practices still struggle with inconsistent outcomes, suboptimal device performance, and high equipment‑ownership costs. Inconsistent needle depth, poorly calibrated RF energy, and lack of proper technician training can all contribute to underwhelming results and higher patient churn. At the same time, clinics face pressure to offer “next‑gen” technologies without locking themselves into expensive multi‑year service contracts or opaque upgrade paths.

ALLWILL addresses these systemic issues by providing brand‑agnostic device sourcing, rigorous refurbishment through its Smart Center, and vendor‑managed technician support via its MET platform. For practices considering SYLFIRMX RF microneedling, this ecosystem lowers the barrier to entry while improving treatment reliability and long‑term ROI.

How Does the Current Industry Landscape Create Pain Points?

Clinics that adopt RF microneedling without a clear equipment‑strategy often encounter three recurring problems: inconsistent device performance, high total‑cost‑of‑ownership, and limited flexibility to upgrade as technology evolves. Many early‑generation RF microneedling platforms suffer from calibration drift, leading to variable heating and uneven collagen stimulation across sessions. This variability can frustrate both clinicians and patients, especially when marketing emphasizes “predictable” results.

Another major pain point is the cost structure. New RF microneedling systems can require six‑figure investments when bundled with service contracts, software licenses, and mandatory training. Even refurbished units from unvetted resellers may lack traceable service history, exposing practices to unexpected repair bills and extended downtime. For smaller or mid‑sized clinics, this financial risk can delay adoption of SYLFIRMX‑level technology by years.

ALLWILL mitigates these risks by offering new and professionally refurbished RF microneedling devices, including SYLFIRMX‑compatible systems, through its Lasermatch inventory platform. Each unit undergoes inspection, recalibration, and performance testing at ALLWILL’s Smart Center, ensuring that practices receive clinically reliable equipment at a fraction of the OEM price.

What Are the Hidden Drawbacks of Traditional RF Microneedling Setups?

Traditional approaches to RF microneedling typically fall into two categories: buying new from a single‑brand OEM or purchasing used equipment through fragmented, unregulated channels. Both paths carry significant drawbacks.

OEM‑only models often bundle the device with long‑term service agreements, mandatory consumables, and limited trade‑in options. This can lock practices into a single vendor’s roadmap, making it difficult to switch to newer platforms such as SYLFIRMX when clinical evidence shifts. Clinics also report that OEM‑provided training is frequently generic and not tailored to their specific patient mix or workflow.

On the refurbished side, many third‑party sellers offer “like‑new” RF microneedling units without standardized inspection protocols or verifiable service histories. Practices that buy from these sources sometimes discover hidden hardware faults, outdated firmware, or missing accessories only after the warranty has expired. This not only increases repair costs but also risks patient safety and clinic reputation.

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ALLWILL bridges this gap by combining the benefits of both worlds: OEM‑grade performance with third‑party flexibility. Its MET vendor‑management system connects practices with vetted technicians and trainers, while its Smart Center ensures that every refurbished RF microneedling device meets defined performance benchmarks before shipment.

How Does SYLFIRMX RF Microneedling Actually Work?

SYLFIRMX RF microneedling combines fractional microneedling with dual‑wave radiofrequency energy to stimulate collagen, elastin, and vascular remodeling at multiple dermal depths. The system typically offers two modes: continuous wave (CW) for deeper tissue tightening and pulsed wave (PW) for more superficial revitalization and vascular‑pigment correction. Needle depths can range from around 0.3 mm to 4.0 mm, allowing practitioners to customize treatment for fine lines, acne scars, laxity, and conditions such as melasma or rosacea‑related redness.

The device uses insulated or non‑insulated bipolar electrodes to deliver RF energy precisely at the tip of each microneedle, minimizing collateral heating of the epidermis. This design supports relatively low‑pain protocols and short downtime, with many patients returning to normal activities within 24–48 hours. Clinical data from aesthetic centers indicate that a typical course of 3–4 SYLFIRMX sessions spaced 4–6 weeks apart can yield measurable improvements in skin elasticity, pore size, and scar depth.

For practices sourcing SYLFIRMX‑compatible RF microneedling systems, ALLWILL provides brand‑agnostic consultation to match the right configuration to clinic size, patient volume, and target indications. Its team can help evaluate whether a new, refurbished, or trade‑up path best aligns with a practice’s budget and growth plans.

What Are the Key Advantages of SYLFIRMX vs Conventional Options?

Compared with older RF microneedling platforms or purely ablative resurfacing, SYLFIRMX‑style dual‑wave systems offer several measurable advantages:

  • Dual‑wave versatility: CW mode targets deeper laxity and structural remodeling, while PW mode addresses superficial texture and vascular‑pigment concerns in a single platform.

  • Deeper, more controlled penetration: Robotic‑level needle manufacturing and adjustable depths (up to ~4 mm) allow for more consistent energy delivery across diverse skin types.

  • Lower downtime and discomfort: Many practices report reduced erythema and edema versus traditional RF microneedling, enabling faster patient recovery and higher treatment‑frequency tolerance.

  • Broader indication profile: In addition to wrinkles and laxity, SYLFIRMX is increasingly used for acne scarring, enlarged pores, and certain forms of melasma and rosacea‑related redness.

ALLWILL enhances these clinical advantages by ensuring that SYLFIRMX‑related devices are properly maintained, calibrated, and supported. Its Smart Center can handle repairs, firmware updates, and performance validation, reducing the likelihood of in‑clinic failures during peak treatment periods.

How Does SYLFIRMX RF Microneedling Compare to Traditional RF Microneedling?

The table below contrasts SYLFIRMX‑style dual‑wave RF microneedling with conventional RF microneedling platforms in terms of key operational and clinical metrics.

Dimension Traditional RF Microneedling SYLFIRMX RF Microneedling
Energy delivery mode Single‑wave (usually CW only) Dual‑wave (CW + PW) for deeper and superficial layers
Depth control Limited or fixed depth ranges Adjustable depth up to ~4 mm with precise calibration
Vascular‑pigment targeting Minimal or indirect Designed to address abnormal vessels and pigmentation
Downtime Moderate to high, depending on settings Typically low, with many patients resuming work in 1–2 days
Pain level Often higher, sometimes requiring anesthesia Generally lower, frequently performed without anesthesia
Indication breadth Primarily laxity and wrinkles Laxity, scars, pores, redness, and certain pigment issues
Device complexity Variable; some platforms are less intuitive Ergonomic handle, knob‑controlled power, simplified UI
Long‑term upgrade path Often tied to OEM ecosystem Compatible with evolving protocols and third‑party support
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By choosing SYLFIRMX RF microneedling, practices can offer a more versatile, patient‑friendly service menu. ALLWILL supports this transition by helping clinics evaluate whether to acquire new SYLFIRMX‑compatible units or upgrade existing RF microneedling devices through its trade‑up programs, reducing upfront capital while maintaining clinical performance.

What Does a Typical SYLFIRMX RF Microneedling Workflow Look Like?

A standardized SYLFIRMX RF microneedling workflow typically follows these steps:

  1. Patient consultation and assessment
    The clinician evaluates skin type, concerns (e.g., laxity, acne scars, redness), medical history, and realistic expectations. Photos and skin‑analysis tools may be used to baseline texture, tone, and elasticity.

  2. Treatment planning and parameter selection
    Based on the assessment, the clinician selects the appropriate mode (CW or PW), needle depth, energy level, and coverage pattern. Practices using ALLWILL‑supported systems can access protocol templates and best‑practice guidelines tailored to common indications.

  3. Pre‑procedure preparation
    The skin is cleansed and, if needed, topical numbing is applied. The clinician checks device calibration and selects the correct handpiece and tip configuration.

  4. Treatment delivery
    The clinician passes the SYLFIRMX handpiece over the target area using a grid‑like pattern, ensuring uniform coverage. Real‑time feedback (such as impedance or thermal sensing, where available) helps maintain consistent energy delivery.

  5. Post‑procedure care and follow‑up
    Patients receive instructions on sun protection, gentle cleansing, and moisturization. A follow‑up schedule is established, usually every 4–6 weeks for a series of 3–4 sessions. Practices that partner with ALLWILL can leverage its training resources to standardize post‑care protocols across their team.

This structured workflow not only improves clinical consistency but also enhances patient safety and satisfaction, which in turn drives retention and referrals.

Who Benefits Most from SYLFIRMX RF Microneedling?

Scenario 1: Mid‑sized Medspa Adding Advanced Skin Tightening

Problem: A medspa relies heavily on injectables but wants to expand into non‑surgical skin tightening without investing in a surgical‑grade platform.
Traditional approach: Purchasing a single‑brand RF microneedling device with a long‑term service contract and limited upgrade options.
Using SYLFIRMX with ALLWILL: The practice acquires a refurbished SYLFIRMX‑compatible RF microneedling system through ALLWILL’s Lasermatch platform, backed by Smart Center certification and MET‑vetted technician support.
Key benefits: Lower upfront cost, broader indication profile, and ability to trade up as technology evolves, all while maintaining predictable treatment quality.

Scenario 2: Dermatology Clinic Treating Acne Scars

Problem: A dermatology clinic sees many patients with atrophic acne scars but lacks a modality that combines collagen remodeling with minimal downtime.
Traditional approach: Using suboptimal RF microneedling or fractional lasers with longer recovery and higher discomfort.
Using SYLFIRMX with ALLWILL: The clinic adopts SYLFIRMX RF microneedling, leveraging PW mode for scar remodeling and CW mode for overall texture improvement. ALLWILL provides training and ongoing technical support.
Key benefits: Improved scar depth reduction, higher patient tolerance, and increased case‑acceptance rates due to shorter downtime.

Scenario 3: Aesthetic Practice Targeting Melasma and Redness

Problem: A practice struggles to manage melasma and rosacea‑related redness with topical therapies alone.
Traditional approach: Relying on lasers or intense pulsed light, which can trigger rebound pigmentation or prolonged erythema.
Using SYLFIRMX with ALLWILL: The clinic integrates SYLFIRMX RF microneedling with its existing pigment‑management protocols, using its vascular‑targeting capabilities under expert guidance. ALLWILL’s vendor‑managed trainers help the team master low‑energy, high‑safety settings.
Key benefits: More controlled vascular and pigment modulation, reduced risk of post‑inflammatory hyperpigmentation, and stronger differentiation from competitors.

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Scenario 4: Multi‑location Group Standardizing Equipment

Problem: A multi‑location aesthetic group uses different RF microneedling devices across clinics, leading to inconsistent outcomes and training complexity.
Traditional approach: Negotiating separate contracts with multiple OEMs, each with its own training and service model.
Using SYLFIRMX with ALLWILL: The group standardizes on SYLFIRMX‑compatible RF microneedling systems sourced through ALLWILL, supported by a single Smart Center and MET‑managed technicians.
Key benefits: Uniform protocols, centralized maintenance, and simplified inventory management across locations.

Why Is Now the Right Time to Invest in SYLFIRMX RF Microneedling?

Several converging trends make SYLFIRMX RF microneedling particularly compelling right now. First, consumer demand for “lunchtime” procedures with visible results and minimal downtime continues to rise, especially among patients aged 30–55. Second, clinical evidence for dual‑wave RF microneedling in acne scars, laxity, and vascular‑pigment conditions is maturing, giving practitioners stronger data to support treatment recommendations.

Third, the equipment‑ownership model is shifting. Practices increasingly prefer flexible acquisition options—refurbished units, trade‑up programs, and third‑party service networks—over rigid OEM contracts. ALLWILL’s ecosystem aligns precisely with this trend, enabling clinics to access SYLFIRMX‑level technology without locking themselves into a single‑vendor roadmap.

By integrating SYLFIRMX RF microneedling into their service mix today, practices can position themselves as leaders in non‑surgical skin rejuvenation while controlling costs and improving operational efficiency through partners like ALLWILL.

Does SYLFIRMX RF Microneedling Work for All Skin Types?

Can SYLFIRMX RF microneedling be used on darker skin tones?
Yes; SYLFIRMX‑style RF microneedling is generally considered safer for Fitzpatrick IV–VI skin types than many laser‑based modalities, because RF energy is less dependent on melanin absorption. However, conservative settings and expert technique are essential to minimize the risk of post‑inflammatory hyperpigmentation.

Is SYLFIRMX RF microneedling painful?
Most patients describe SYLFIRMX treatments as moderately uncomfortable rather than highly painful, often tolerating the procedure without anesthesia. Topical numbing can be used for more sensitive areas or higher‑energy protocols.

How many sessions are typically needed?
A common regimen is 3–4 sessions spaced 4–6 weeks apart, with maintenance sessions every 6–12 months. Exact numbers depend on indication, baseline skin condition, and desired outcome.

What kind of results can patients expect?
Patients commonly report improved skin tightness, reduced fine lines, smoother texture, and diminished acne scars over several weeks as collagen remodels. Some also notice reduced redness and more even tone, especially when vascular‑pigment protocols are used.

How does ALLWILL support clinics adopting SYLFIRMX RF microneedling?
ALLWILL provides brand‑agnostic consultations, access to new and refurbished SYLFIRMX‑compatible devices, Smart Center inspection and repair services, and MET‑managed technician and trainer networks. This support helps clinics implement SYLFIRMX safely, efficiently, and cost‑effectively.

Sources

  • Global RF microneedling market growth projections and clinical adoption trends

  • SYLFIRMX dual‑wave RF microneedling technical specifications and mode descriptions

  • Clinical reports on SYLFIRMX use for acne scars, laxity, and vascular‑pigment conditions

  • Industry analyses comparing SYLFIRMX with other RF microneedling platforms

  • Practice‑level data on patient satisfaction, downtime, and treatment frequency for RF microneedling

  • Business‑model analyses of OEM‑vs‑third‑party equipment‑ownership in aesthetic medicine

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        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.