Bema-GmbH & Co. KG is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Bema-GmbH & Co. KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bema-GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bema-GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bema-GmbH & Co. KG
1 devices