Monday, June 1
Registration Open (CEO-Only Forum)
CEO-Only Forum
The inaugural CEO-Only Forum @ Medtech MVP is an exclusive gathering for 100 current Medtech CEOs from venture-backed medical device start-up companies. It brings together first-time founders and seasoned serial entrepreneurs in a setting where everyone participates, asks questions, and learns from one another.
This is an optional opportunity for CEOs only. See CEO-Only Forum page on the conference website for more details.
Registration Open (Medtech MVP)
Organizer's Welcome Remarks
PANEL DISCUSSION:How Medtech Incumbents Scale Innovation through M&A and Partnerships
Jon Salveson, Vice Chairman, Healthcare Investment Banking, Piper Sandler
Large MedTech operating companies sit at the center of complex global ecosystems—balancing R&D productivity, regulatory rigor, manufacturing scale, and commercial execution across diverse markets. In this M&A and partnerships-focused discussion, senior leaders from established operators unpack where innovation truly matters inside large organizations, how priorities are set, and what it takes to move from promising technology to scaled impact across portfolios and geographies.
•Where are large MedTech incumbents actively looking to acquire, partner, or invest today—and why?
•What clinical, commercial, or strategic gaps are driving current M&A and BD roadmaps?
•What signals differentiate a “must-buy” asset from a technology that remains a long-term partnership or pilot?
•How do incumbents evaluate build vs. buy vs. partner decisions across platforms, point solutions, and enabling technologies?
•What are the most common deal-breakers that stall or kill acquisition discussions?
•How do large operators assess scalability, reimbursement readiness, and integration risk before moving forward?
•What should founders understand about timing, internal champions, and proof points to align with acquisition windows?
Chris Eso, Vice President & Global Head, Corporate & Business Development, M&A, Ventures, Medtronic Inc.
AVIO Medtech Consulting, in partnership with the Destination Medical Center Fredrikson, F&N Med and Mobius Medical, announces that three finalists have been selected for the 2026 AVIO Medtech MVP Pitch Contest.
Meet the finalists:
Bairitone Health
Bairitone Health is developing Somnar, a non-invasive wearable platform for obstructive sleep apnea assessment that uses passive sonar technology and a facial patch to characterize airway obstruction during natural sleep. The company recently received FDA Breakthrough Device Designation for the platform.
LIQID Medical
LIQID Medical is developing novel ocular implants for glaucoma treatment, including its OptiShunt device, designed to improve fluid drainage in the eye and address a leading cause of irreversible vision loss worldwide.
Entirety Biomedical
Entirety Biomedical is developing absorbable magnesium implant systems for orthopedic fixation using its proprietary Curasorb alloy technology. The company recently announced seed financing to advance the platform toward first-in-human clinical trials.
As Medtech MVP celebrates its 25th Anniversary, this special recognition brings together a group of long-standing advisors and industry leaders who have helped shape the event and the broader medtech ecosystem over the years. Join us as we acknowledge their contributions, reflect on the evolution of the industry, and recognize the relationships, ideas, and leadership that have helped define Medtech MVP over the past quarter century.
Transition to Breakout Sessions
BREAKOUT DISCUSSION:Closing the MedTech Narrative Gap: Strategic Cinematic Film as a Commercialization Engine
John Haagen, CEO & Co-Founder, VISUM
VISUM explores the MedTech Narrative Gap—the disconnect between clinical innovation and market understanding. Through select film examples and a deeper case study featuring an emerging Series B MedTech disruptor, learn how cinematic films built around authentic clinical voices, real clinical environments, and 3D visualization align teams and accelerate understanding. These strategic assets strengthen clinician adoption, build investor confidence, and drive commercialization.
BREAKOUT DISCUSSION:Real-World Lessons from MedTech CEOs Who Have Navigated Funding, FDA Approval, and First-in-Human Trials
Experienced MedTech CEOs share lessons from navigating funding, FDA approval, and first-in-human trials, highlighting clinical strategy decisions that help de-risk development and accelerate company growth.
Networking Welcome Reception

Close of Day
Tuesday, June 2
Registration and Morning Coffee
Organizer's Welcome Remarks
Medtech MVP 2026 Award & Fireside Chat: Inside Conformal Medical's Acquisition by W.L. Gore & Associates
How Health Systems are Adopting Robotics across Care Settings
Virginia L. Giddings, PhD, Vice President, Exploration, Edwards Lifesciences
Health systems are evaluating robotics not only for surgical precision, but also for their potential to address workforce shortages, improve efficiency, and enhance care delivery across multiple settings. From the operating room to inpatient units, rehabilitation, logistics, and remote care, this session examines where robotics are delivering real value and what it takes to scale adoption across the healthcare enterprise.
BREAKOUT DISCUSSION:Escalation Options for FDA Submissions
Learn how to manage your FDA submission review when things go sideways. This session covers practical escalation strategies for 510(k), De Novo, and PMA submissions: when to involve FDA management, how to communicate concerns effectively, and when informal versus formal appeals make sense—while preserving the relationship.
Networking Coffee Break
PANEL DISCUSSION:From Approval to Adoption: Evidence, Reimbursement, and Commercial Strategy in Medtech
Jolayne Devers, Partner, JD Lymon Group
Evidence generation is a critical driver of reimbursement and commercial success in Medtech. Too often, studies are designed to achieve FDA approval but fall short of supporting payer coverage and wide-spread adoption. This panel explores how companies, payers, and investors think about evidence across the product lifecycle—and how FDA strategies, CMS fit-for-purpose studies, and real-world evidence can better align reimbursement strategy with commercialization goals.
What types of evidence matter most to commercial and government payers when making coverage and reimbursement decisions?
How early should Medtech companies align evidence generation with reimbursement and commercial strategy?
Where do companies most often fall short in generating evidence that supports coverage?
How are real-world evidence and alternative study designs influencing payer adoption today?
What practical steps can companies take to better align evidence generation, reimbursement, and go-to-market strategy?
Roundtable Discussions are informal, moderated discussions, allowing participants to exchange ideas and experiences and develop future collaborations around a focused topic. Each discussion will be led by a facilitator who keeps the discussion on track and the group engaged. To get the most out of this format, please come prepared to share examples from your work, be a part of a collective problem-solving session, and participate in active idea sharing.
Roundtables 1 & 2: FDA Submission Strategies
Mark DuVal, CEO, DuVal & Associates
Bryan Feldhaus, President, DuVal & Associates
Chris Lyle, Vice President, Evidence Development & Health Economics, DuVal & Associates
Roundtables 3 & 4: Leveraging Film to Drive Commercialization
John Haagen, Co-Founder and CEO, VISUM
Jordan Haagen, Co-Founder and Lead Producer, VISUM
Roundtables 5 & 6: What Gets Funded in Medtech Today
Petra Gorombei, Investment Professional, Vensana
Allison Kind, Investment Professional, Vensana
Roundtables 7 & 8: The Future of Surgical Robotics
Kate Jackson Hobbs, VP, Corporate Development Strategy, Intuitive
Maggie Nixon, CEO, Capstan Medical
IN-PERSON ONLY BREAKOUT:LUNCHEON PRESENTATION: Capital-Raising and Strategic M&A Considerations for Growth-Stage Medtech Companies
Hear insights and learnings from industry professionals across the strategic and growth-stage medtech landscape. When is too early to engage with strategics? Who are the right groups to talk to? Is Corporate Venture Capital (CVC) still an option and what are they looking for? How should companies be thinking about financing in a world where timelines to exit are getting longer? Find answers to all of these questions and more as J.P. Morgan moderates a diverse panel on capital raising and strategic M&A considerations for growth-stage medtech companies.
From Start-up to Scale-up: What it Took to Reach Mid-Stage—And What Comes Next
Lori Chmura, CEO, Leadership, Nyra Medical
Reaching mid-stage is a defining milestone for Medtech companies—but scaling beyond it presents new operational, regulatory, and capital challenges. This CEO-led discussion explores the decisions, tradeoffs, and inflection points that shaped their growth, including how geography, talent hubs, and ecosystem support influenced their trajectory.
Oncology Innovation: FDA Cleared, AI-Enabled, Separately Billable, Recurring Revenue
Eric Horler, President and CEO, AIQ Solutions
AIQ Solutions has commercialized an FDA-cleared, AI-enabled software medical device with a recurring revenue model. Targeting the most complex oncology patients — those with metastatic disease — AIQ's technology-enabled service improves treatment decisions while reducing expenditures on high-cost therapeutics. A separately billable CPT code, strong clinical data, and high payer return on investment are driving accelerating commercial demand.
Networking Refreshment Break
Investing in Medtech Now: Where Capital is Moving—and Why
Maria Berkman, MD, MBA, Partner, Vensana Capital
Capital deployment in Medtech is becoming more selective as investors prioritize evidence, differentiation, and scalable economics. This investment-focused panel examines current deal dynamics, valuation expectations, and where investors see the most compelling opportunities across devices, diagnostics, robotics, and digital-enabled Medtech.
Tech Inside Medtech: How AI Platforms are Powering the Next Generation of Devices
Alexander Schmitz, Partner, Endeavour Vision
As Medtech companies integrate advanced AI into regulated products, partnerships with large technology platforms are becoming critical. This session brings together leaders from Medtech and major technology companies to explore how AI, computing power, and digital infrastructure are reshaping device development, clinical performance, and commercialization—while navigating regulatory and operational complexity.
Closing Networking Reception

Close of Summit
CONFERENCE CONTENT
Ben Lakin, PhD
Chief Executive Officer
(+1) 781-972-5454
blakin@cambridgeinnovationinstitute.com
Jason Green
Senior Conference Director
jgreen@cambridgeinnovationinstitute.com
PARTNERING & SPONSORSHIP
Brian Caine
Manager, Strategic Partnerships
Venture, Innovation & Partnering (VIP) Event Series
(+1) 908-809-0946
bcaine@cambridgeinnovationinstitute.com