Medical Device Manufacturer · DE , Neu-Ulm

Zimmer Medizinsysteme GmbH - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2016

Total

Cleared

Denied

FDA 510(k) Regulatory Record - Zimmer Medizinsysteme GmbH General & Plastic Surgery ✕

3 devices

1-3 of 3

Regulatory consultants 510(k) submission support ecosystem

Quality and Regulatory Services

Qara Consulting

Qara Consulting, LLC

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026