ZuriMED Technologies AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
ZuriMED Technologies AG - FDA 510(k) Cleared Devices
Recent clearances: FiberLocker Implant, FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN)
2
Total
2
Cleared
0
Denied
ZuriMED Technologies AG has 2 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Latest FDA clearance: Jan 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by ZuriMED Technologies AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - ZuriMED Technologies AG
2 devices