Berchtold GmbH & Co. KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Berchtold GmbH & Co. KG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Berchtold GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Charleston, US.
Historical record: 2 cleared submissions from 2009 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Berchtold GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Berchtold GmbH & Co. KG
2 devices