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.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
2 devices