Breaking News: Our FiberLocker® System has just received FDA clearance!
We’re more than thrilled to announce that our innovative FiberLocker® System has officially received FDA 510(k) clearance! This major milestone marks a significant step forward for ZuriMED and for advancing rotator cuff repair technology overall.
This means that the FiberLocker® System will enter the U.S. market in Q1 2025, and we eagerly anticipate the first clinical application. Our solution directly addresses the needs of physicians and patients, with the goal to reinforce rotator cuff repairs and improve traditional techniques.
The whole team has worked many years for this moment, and we are more than proud to showcase our innovative technology to the world now. A big thank you to our partners, supporters, and everyone who has contributed to this journey!
FDA Clearance for FiberLocker® System
