Medical Device Manufacturer · US , South Bend , IN

Heraeus Kulzer,GmbH - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2004

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Heraeus Kulzer,GmbH Orthopedic ✕

3 devices

1-3 of 3

Cleared Sep 14, 2005

Orthopedic · 244d

Cleared Jul 07, 2005

Orthopedic · 94d

Cleared Jul 07, 2005

Orthopedic · 94d