ZuriMED Technologies AG - FDA 510(k) Cleared Devices
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.
FDA 510(k) cleared devices by ZuriMED Technologies AG
2 devices