Osstell AB is one of 26038 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osstell AB - FDA 510(k) Cleared Devices
Recent clearances: Reusable SmartPeg, Osstell Beacon, Osstell IDx
5
Total
5
Cleared
0
Denied
Osstell AB has 5 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Latest FDA clearance: Sep 2026. Active since 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osstell AB Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Msquared Associates, Inc. and ProPharma Group.
FDA 510(k) Regulatory Record - Osstell AB
5 devices