Osstell AB - FDA 510(k) Cleared Devices
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.
FDA 510(k) cleared devices by Osstell AB
4 devices