Suzen Dubre

Chief Executive Officer and Co-Owner at Marins Med LLC

Role: Chief Executive Officer at Marins, Inc
Location: Georgetown, DE, US
LinkedIn followers: 500 followers

General Business & ManagementView LinkedIn profile

About Suzen Dubre

I’m the CEO and co-founder of Marins Inc, where we design prosthetic technology built…

Experience

Chief Executive Officer
Marins, Inc
Jan 2021 — Present · DE, US
Leading the development and commercialization of breakthrough prosthetic technologies for upper extremity amputees. Spearheaded R&D efforts resulting in our patented ProHensor® terminal device, which revolutionizes body-powered prosthetic functionality through innovative engineering solutions.Built the company from concept to market-ready products, overseeing all aspects of business development, regulatory compliance, and strategic partnerships within the medical device industry. Established relationships with prosthetists, rehabilitation centers, and healthcare providers to ensure our innovations reach those who need them most.Managed cross-functional teams in product design, clinical testing, and manufacturing while securing intellectual property protections and navigating FDA regulatory pathways. Successfully positioned Marins Med as an emerging leader in assistive technology innovation.Key Achievements- Developed and patented proprietary prosthetic terminal device technology- Built strategic partnerships across the prosthetics and rehabilitation ecosystem- Led product development from prototype through clinical validation- Established regulatory compliance framework for medical device commercialization

Contact information

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Current company

Marins, Inc

Medical Equipment Manufacturing · 3 employees · Founded 2021 · Georgetown, Delaware, United States

Marins, Inc. is a Delaware-based medical device company and the developer of the ProHensor® VCAL, the world\'s first modular, voluntary-closing auto-locking terminal device for upper-limb amputees. The ProHensor VCAL was invented by an upper-limb amputee who built the device he could not find on the market. That origin shapes everything we do: the engineering decisions, the clinical partnerships, and the standard we hold ourselves to. When the inventor is also the user, the feedback loop is closed in a way no focus group can replicate. The device is FDA registered, protected by U.S. patents through 2041, and CE marked for the European market. It is available directly to certified O&P clinicians in the United States. Users have also been fitted internationally through humanitarian prosthetic programs, reflecting the device\'s reach beyond traditional commercial channels. We work with prosthetists and the amputee community to ensure every design choice translates into real-world function, confidence, and durability. Our focus is singular: get the most capable body-powered terminal device in history to the people who need it most.

marinsmed.com

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