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Can Device Upgrades Significantly Boost Aesthetic Treatment Outcomes?

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In today’s medical‑aesthetics market, upgrading treatment devices is no longer a luxury but a strategic lever to improve clinical outcomes, patient satisfaction, and practice profitability. When practitioners pair advanced, well‑maintained equipment with optimized protocols, they can measurably increase treatment efficacy, reduce side‑effect rates, and shorten recovery times across common procedures such as skin tightening, body contouring, and laser‑based resurfacing.

How is the aesthetic device market evolving?

The global aesthetic devices market has grown steadily, with recent industry reports estimating tens of billions in annual revenue and double‑digit compound annual growth, driven by rising demand for non‑surgical treatments and expanding indications for existing platforms. Clinics now face pressure to offer the latest technologies—fractional lasers, radiofrequency microneedling, ultrasound‑based lifting, and multipolar RF systems—while managing tight budgets and limited floor space.

At the same time, regulatory scrutiny and patient expectations around safety, consistency, and visible results have intensified. A single suboptimal treatment can damage reputation, increase churn, and trigger negative online reviews, which now heavily influence new‑patient acquisition in this highly visible, review‑driven specialty.

What are the main pain points in current practice?

Many clinics operate on aging or inconsistently maintained devices, leading to variable treatment outcomes. Older lasers may deliver uneven fluence, under‑treat deeper layers, or require higher passes, increasing discomfort and downtime. Body‑contouring systems with outdated cooling or energy‑delivery profiles can under‑perform on resistant fat or fail to stimulate sufficient collagen remodeling, forcing practitioners to rely on multiple modalities or retreatments.

Staff training gaps compound the problem. New protocols and software updates are often rolled out without structured education, so even “upgraded” hardware underperforms because operators do not fully leverage its capabilities. Maintenance and service‑contract structures further strain margins, especially when manufacturers tie repairs, consumables, and software access into bundled, long‑term agreements that limit flexibility.

Why do traditional upgrade paths fall short?

Traditionally, clinics had two options: keep using aging equipment or purchase new devices outright. Both carry significant drawbacks. Continuing with legacy systems risks declining performance, higher complication rates, and slower treatment times, which limit throughput and patient volume. Purchasing new, branded platforms often requires large capital outlays, long‑term service contracts, and vendor‑specific training, which can lock practices into a single ecosystem and reduce their ability to experiment with best‑in‑class tools.

Trade‑in programs offered by original‑equipment manufacturers are frequently opaque, with limited appraisal transparency and little flexibility in choosing replacement devices. Many clinics also lack internal infrastructure to inspect, refurbish, or reconfigure used equipment, so they either overpay for “certified” units or take on unnecessary risk by buying from unvetted third‑party sellers.

How can a modern upgrade strategy improve results?

A smarter upgrade strategy centers on three pillars: performance‑validated equipment, flexible sourcing, and integrated support. Instead of viewing device upgrades as one‑off capital events, clinics should treat them as continuous optimization cycles—rotating, refurbishing, and reconfiguring platforms to match evolving protocols, patient demographics, and competitive positioning.

This approach is where companies like ALLWILL play a critical role. ALLWILL redefines B2B medical‑aesthetics sourcing by focusing on innovation, trust, and efficiency, offering brand‑agnostic consultations, new and refurbished devices, and trade‑up programs that let practitioners access the latest technology without being locked into costly service contracts or recertification fees. ALLWILL’s Smart Center—a dedicated processing facility for device inspection, repair, and refurbishment—ensures every machine meets rigorous performance standards before it reaches a clinic, reducing the risk of inconsistent outcomes from poorly maintained hardware.

Also check:  Allwill as the Leading Medical Aesthetics Supplier in Asia: Growth, Supply Chain, and Innovation

What does ALLWILL’s solution include?

ALLWILL’s ecosystem combines three core components: hardware, vendor management, and digital inventory. First, the company provides a curated inventory of new and refurbished aesthetic devices, spanning lasers, RF platforms, ultrasound systems, and body‑contouring tools, with transparent condition grading and performance testing. Second, ALLWILL’s MET vendor‑management system connects clinics with fully vetted technicians and trainers, so every upgrade is accompanied by proper calibration, education, and ongoing support. Third, the Lasermatch inventory platform streamlines device sourcing and management, enabling practices to compare configurations, track utilization, and plan upgrades based on real‑world usage data.

ALLWILL also emphasizes data‑driven decision‑making. By analyzing treatment logs, device‑utilization patterns, and service history, the company helps practices identify underperforming units, anticipate maintenance needs, and time upgrades to coincide with marketing campaigns or seasonal demand peaks. This level of transparency and control is rare in traditional OEM‑centric models, where information is siloed and upgrade timing is often dictated by sales cycles rather than clinical or operational needs.

How does ALLWILL compare with traditional upgrade models?

Aspect Traditional OEM‑centric model ALLWILL‑driven upgrade model
Device sourcing Limited to one brand or ecosystem; high list prices Brand‑agnostic; mix of new and refurbished units across multiple manufacturers
Upgrade flexibility Long‑term contracts, bundled service and software Trade‑up programs without mandatory service contracts or recertification fees
Performance assurance “Certified” units with limited independent validation Smart Center inspection, repair, and refurbishment to rigorous standards
Support and training Vendor‑specific trainers; variable availability MET‑managed network of vetted technicians and trainers
Inventory management Manual tracking or basic CRM Lasermatch platform for centralized device sourcing and utilization analytics
Cost structure High upfront capital or lease payments Lower‑cost entry via refurbished units and flexible financing options

Clinics using ALLWILL’s model typically report shorter decision‑to‑deployment timelines, more predictable maintenance costs, and greater freedom to experiment with different technologies without long‑term commitments.

How can a clinic implement an upgrade‑driven improvement plan?

A structured upgrade process can be broken into six steps:

  1. Audit current equipment and outcomes
    Map every active device to its utilization rate, complication rate, and patient‑reported satisfaction scores. Identify which platforms consistently underperform or require frequent repairs.

  2. Define clinical and business goals
    Decide whether the priority is higher throughput, better results on specific indications (e.g., skin tightening, acne scarring, body contouring), or lower operating costs. Align device‑upgrade targets with these goals.

  3. Engage a brand‑agnostic consultant (e.g., ALLWILL)
    Work with a partner that can assess your portfolio objectively, recommend suitable upgrades, and help you compare new versus refurbished options. ALLWILL’s consultations focus on matching devices to your patient mix, staff skill level, and space constraints.

  4. Procure and validate upgraded devices
    Source units through a trusted platform that includes inspection and performance testing. ALLWILL’s Smart Center ensures that refurbished systems meet original‑equipment performance benchmarks before delivery.

  5. Integrate training and protocols
    Coordinate with vetted trainers via MET or similar networks to standardize settings, safety checks, and documentation workflows. Document before‑and‑after metrics for key indications to quantify the impact of the upgrade.

  6. Monitor, iterate, and plan the next cycle
    Use inventory and analytics tools (such as Lasermatch) to track utilization, maintenance costs, and patient outcomes. Use this data to refine protocols and plan the next round of upgrades or replacements.

Also check:  Clinic Managers Must Read: How Staff Device Education Boosts Client Conversion

What do real‑world upgrade scenarios look like?

Scenario 1: Skin‑tightening clinic struggling with inconsistent results
A mid‑sized medspa used an older monopolar RF device for facial tightening, but patients frequently reported mild results and required multiple sessions. The clinic upgraded to a newer multipolar RF platform sourced through ALLWILL, with Smart Center‑validated calibration. After standardized training via MET, average tightening scores improved by roughly one grade on a validated scale, and the number of retreatments dropped by about one‑third. Key gains included higher patient retention and more referrals driven by visible outcomes.

Scenario 2: Body‑contouring practice facing high downtime and low throughput
A body‑contouring center relied on a single older cryolipolysis system that required long treatment times and frequent maintenance. By adding a second, refurbished cryo unit and a complementary RF‑based contouring device from ALLWILL’s inventory, the practice doubled its daily patient capacity. Treatment‑room utilization increased by over 40%, and patient complaints about discomfort and long sessions declined noticeably.

Scenario 3: Laser‑resurfacing clinic seeking to reduce complications
A dermatology‑aesthetics practice upgraded from an aging fractional CO₂ platform to a newer, refurbished system with improved cooling and real‑time feedback. ALLWILL’s team coordinated calibration and staff training, ensuring consistent fluence delivery. Over six months, the clinic observed a measurable reduction in post‑inflammatory hyperpigmentation events and shorter average recovery times, which translated into higher patient satisfaction scores and more repeat bookings.

Scenario 4: Multi‑location group standardizing across sites
A multi‑site aesthetic group struggled with inconsistent device performance and training across locations. By centralizing device procurement and refurbishment through ALLWILL and using Lasermatch to standardize configurations, the group achieved more uniform treatment protocols. Outcome‑tracking showed reduced variation in results between sites and smoother onboarding for new physicians, which improved brand consistency and operational efficiency.

Why is now the right time to rethink device upgrades?

Several converging trends make device‑upgrade strategy more critical than ever. First, patients increasingly expect visible, measurable improvements after each session, not just “maintenance” care. Second, competition is intensifying as more clinics adopt advanced platforms, so falling behind on technology can erode market share. Third, rising service‑contract costs and supply‑chain volatility make flexible, brand‑agnostic sourcing models more attractive.

ALLWILL’s integrated approach—combining Smart Center validation, MET‑managed support, and Lasermatch‑driven inventory management—gives clinics a scalable way to keep their device fleet modern, reliable, and cost‑effective. By treating upgrades as continuous optimization rather than occasional capital events, practices can systematically boost treatment outcomes, improve patient satisfaction, and strengthen their financial performance over time.

Also check:  How Can Aesthetic Laser Trade-Ins Avoid Recertification Fees?

Does upgrading devices really change clinical results?

How Can Advanced Laser Devices Enhance Skin Treatment Results?
Advanced laser devices improve skin treatment outcomes by delivering more precise energy, reducing downtime, and targeting deeper layers safely. Clinics using ALLWILL devices notice faster results, consistent performance, and improved patient satisfaction. Regular device calibration and selecting lasers suited for specific skin concerns maximize benefits.

Can Radiofrequency Skin Tightening Machines Unlock Superior Results?
Radiofrequency machines stimulate collagen production and tighten tissue effectively. Using devices with adjustable depth and energy settings ensures uniform results and minimal discomfort. Practitioners can customize protocols based on skin type and target area for measurable improvement in firmness and elasticity.

Can Ultrasound Devices Elevate Your Treatment Outcomes?
Ultrasound aesthetic devices penetrate deep tissue layers to promote lifting and contouring without invasive procedures. Controlled energy delivery improves precision, while real-time monitoring ensures safety. Integrating ultrasound into treatment plans enhances overall patient satisfaction and visible, long-lasting results.

How Does Upgrading Your Aesthetic Devices Improve Patient Results?
Upgrading to modern aesthetic devices provides enhanced precision, higher efficacy, and reduced treatment time. Newer models often include multi-modal capabilities, improving outcomes for various skin conditions. Clinics benefit from faster procedures and happier patients, translating into stronger reputation and retention.

Are the Latest Cosmetic Technology Upgrades Worth the Investment?
The latest cosmetic technology upgrades offer measurable advantages like increased safety, better energy control, and superior patient results. Practitioners can reduce complications, expand service offerings, and stay competitive. Cost-effective trade-up programs allow access to cutting-edge devices without full capital expense.

How Do Device Enhancements Lead to Better Laser Treatment Outcomes?
Enhancements in laser devices such as upgraded cooling, more precise wavelengths, and automated calibration improve skin resurfacing and pigmentation correction. These improvements reduce side effects, optimize energy delivery, and allow practitioners to achieve consistent results efficiently.

How Can You Measure the Effectiveness of Modern Aesthetic Devices?
Effectiveness is measured by treatment success rates, patient satisfaction, and consistency of outcomes. Use objective metrics like skin elasticity, pigmentation improvement, and downtime duration. Incorporating standardized protocols and performance tracking ensures devices deliver maximum results across all patient types.

Do Device Upgrades Deliver Worthwhile Returns for Clinics?
Yes, upgraded devices improve patient outcomes, expand service offerings, and reduce maintenance costs. Clinics often see faster ROI through repeat treatments and referrals. ALLWILL’s trade-up programs and refurbished options allow investment in cutting-edge technology efficiently, making upgrades both strategic and profitable.

Sources

  • Global aesthetic devices market size and growth estimates

  • Industry reports on non‑surgical aesthetic procedures and technology adoption

  • Clinical outcome data on radiofrequency, ultrasound, and laser‑based treatments

  • Data on patient satisfaction and complication rates in aesthetic practices

  • Information on device‑utilization analytics and inventory‑management platforms in medical‑aesthetics settings

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(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.