Heraeus Kulzer GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Heraeus Kulzer GmbH & Co. KG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Heraeus Kulzer GmbH & Co. KG has 4 FDA 510(k) cleared medical devices. Based in Hanau, DE.
Historical record: 4 cleared submissions from 2003 to 2004. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Heraeus Kulzer GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Heraeus Kulzer GmbH & Co. KG
4 devices