Sivantos GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Sivantos GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sivantos GmbH has 1 FDA 510(k) cleared medical devices. Based in Erlangen, DE.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Sivantos GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sivantos GmbH
1 devices