Medical Device Manufacturer · DE , Hanau

Heraeus Kulzer GmbH & Co. KG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

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

1-4 of 4