Sopro-Comeg GmbH is one of 199 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Sopro-Comeg GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sopro-Comeg GmbH has 1 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Sopro-Comeg GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sopro-Comeg GmbH
1 devices