3D Systems and TISSIUM Achieve FDA Approval for Innovative 3D-Printed Peripheral Nerve Repair Solution
3D Systems Corporation, in collaboration with French MedTech company TISSIUM, has achieved a significant milestone with the FDA's De Novo marketing authorization for their innovative 3D-printed medical device aimed at regenerative repair of peripheral nerve damage. This first-of-its-kind, bioabsorbable device, known as COAPTIUM® CONNECT with TISSIUM Light, leverages TISSIUM's proprietary biomorphic programmable polymers and 3D Systems' advanced bioprinting technologies. The approval marks a transformative step in patient care, offering a sutureless, atraumatic solution for nerve repair. This achievement underscores the partnership's success in pioneering regenerative medical solutions and sets a new industry standard for high-resolution elastomeric medical implants.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 3D Systems Corporation published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9484713-en) on June 26, 2025, and is solely responsible for the information contained therein.
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