Osstell AB is one of 5511 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: Osstell Beacon
4
Total
4
Cleared
0
Denied
Osstell AB has 4 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Historical record: 4 cleared submissions from 2008 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osstell AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Osstell AB
4 devices