Surgical Fusion Technologies GmbH is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Surgical Fusion Technologies GmbH - FDA 510(k) Cleared Devices
Recent clearances: SF Push-in Anchor, SF Push- in Anchor
2
Total
2
Cleared
0
Denied
Surgical Fusion Technologies GmbH has 2 FDA 510(k) cleared medical devices. Based in Schlieren, CH.
Latest FDA clearance: Mar 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Surgical Fusion Technologies GmbH 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 - Surgical Fusion Technologies GmbH
2 devices