
Our Mission
VerAvanti was founded to address a fundamental limitation in endoscopic imaging. Many of today’s devices were designed decades ago, relying on side-view visualization and reusable systems that can limit workflow efficiency and introduce operational challenges in modern clinical environments.
In collaboration with the University of Washington, VerAvanti developed the patented Scanning Fiber Endoscope (SFE), a new approach to endoscopic imaging designed to deliver high-quality visualization through ultra-small, single-use devices.
Our focus is to enable physicians to see more clearly, work more efficiently, and make better-informed decisions during minimally invasive procedures. By combining precision engineering with a commitment to patient safety and clinical practicality, VerAvanti is building imaging technologies designed for the needs of modern healthcare.
VerAvanti is currently pursuing 510(k) clearance by the U.S. Food and Drug Administration (FDA) and preparing to expand production and introduce our diagnostic solutions worldwide. Committed to ongoing innovation, we aim to improve healthcare standards by making procedures safer, faster, and more effective for both patients and providers.
The Timeline


1
Foundational Research and Collaboration
Laying the groundwork for groundbreaking technology.
Initial research began in collaboration with the University of Washington, forming the basis for our fiber-optic endoscopy innovations.
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2
Prototype Testing and Validation
Ensuring safety and effectiveness through testing.
Early SFE prototypes were tested in laboratory, preclinical and early research studies at the University of Washington.


3
Exclusive License
Protecting our technology through comprehensive patents.
Protected by an exclusive worldwide license from the University of Washington and a portfolio of issued patents.
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4
Final Production Model Established
Refining the design for scalability and precision.
VerAvanti built its own manufacturing capability in Bothell, including a cleanroom, to produce its catheters at scale.


5
510(k) Submission and Launch
Bringing VerAvanti’s innovations to healthcare providers.
VerAvanti expects to submit its first 510(k), for Luce, in 2027, with U.S. launch following clearance.
Leadership

Gerald McMorrow
Founder and CEO

Luis Savastano
Chief Medical Officer

Juan Vegarra
Chief Revenue Officer and Acting Chief Financial Officer

Jason Capodanno
Chief Operating Officer
Clinical Advisors

Patrick McVeigh, MD
MD

Mark Reisman
Clinical Professor of Medicine

William Lombardi
Associate Clinical Professor of Medicine

John Petersen
Director of Cardiovascular Research

Gerald McMorrow
Chairman of the Board

Fred Moll
M.D., Founder and CEO of Auris Health

David C. Auth
Ph.D, Affiliate Professor of Bioengineering

Michael Moyer
Board Member


