Medical 21

Medical 21

Is this your company? Claim your profile to update info and connect with investors.
Claim profile

Private Company

Funding information not available

Overview

Medical 21 is a private, pre-revenue medical device innovator targeting a fundamental limitation in cardiovascular surgery: the need for vessel harvesting in bypass procedures. The company's core technology is the MAVERICS Graft, a biocompatible, nitinol-scaffold-based implant that leverages the body's regenerative pathways to guide the formation of a new, arterial-like blood vessel. By providing an off-the-shelf synthetic graft, Medical 21 seeks to expand patient eligibility, reduce procedure time and complications, and improve outcomes for the millions of patients undergoing CABG surgery worldwide, a field that has seen little innovation for over 60 years.

Cardiovascular DiseaseCoronary Artery Disease

Technology Platform

Regenerative synthetic graft platform utilizing a nitinol scaffold designed to stimulate angiogenesis and guide the body's formation of a new, arterial-like blood vessel for bypass procedures.

Opportunities

Medical 21 addresses a massive, stagnant market with a potential paradigm-shifting technology.
The opportunity lies in eliminating vessel harvesting morbidity, expanding the eligible patient pool to include those with diabetes or poor vasculature, reducing surgical time and cost, and improving long-term graft patency rates compared to harvested veins.
Success could capture a significant portion of the global CABG market.

Risk Factors

Key risks include the high technical and clinical risk of proving the graft's long-term efficacy and safety in humans, a formidable regulatory pathway for a novel Class III device, and the commercial challenge of changing deeply entrenched surgical practices.
The company is also pre-revenue and reliant on external funding.

Competitive Landscape

Direct competition for an off-the-shelf, small-diameter coronary graft is limited, as no such product is commercially available. The primary competition is the entrenched standard of care: autologous vessel harvesting (internal mammary artery, saphenous vein). Indirect competition includes other emerging tissue engineering approaches, drug-eluting stents for less severe disease, and other companies researching biohybrid or fully tissue-engineered vascular grafts, though none have reached the coronary market.