Botiss Biomaterials GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Botiss Biomaterials GmbH - FDA 510(k) Cleared Devices
Recent clearances: Jason membrane
1
Total
1
Cleared
0
Denied
Botiss Biomaterials GmbH has 1 FDA 510(k) cleared medical devices. Based in Zossen, DE.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Botiss Biomaterials GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Botiss Biomaterials GmbH
1 devices