Medical Device Manufacturer · DE , Neu-Ulm

Zimmer Medizinsysteme GmbH - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2016
13
Total
13
Cleared
0
Denied

Zimmer Medizinsysteme GmbH has 13 FDA 510(k) cleared medical devices. Based in Neu-Ulm, DE.

Latest FDA clearance: Jan 2026. Active since 2016. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Zimmer Medizinsysteme GmbH Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Quality and Regulatory Services, Qara Consulting and Qara Consulting, LLC.

FDA 510(k) Regulatory Record - Zimmer Medizinsysteme GmbH
13 devices
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