Medical Device Manufacturer · DE , 7910 Neu-Ulm, Germany

Zimmer Elektromedizin GmbH - FDA 510(k) Cleared Devices

12 submissions · 8 cleared · Since 1985

Recent clearances: CRYOMINI, CRYO, MODEL V6.0, GALVA 5-T

12
Total
8
Cleared
0
Denied

Zimmer Elektromedizin GmbH has 8 FDA 510(k) cleared medical devices. Based in 7910 Neu-Ulm, Germany, DE.

Historical record: 8 cleared submissions from 1985 to 2008. Primary specialty: Physical Medicine.

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

Regulatory submissions have been managed by Tuv America, Inc. and Tuv Sud America, Inc..

FDA 510(k) Regulatory Record - Zimmer Elektromedizin GmbH

12 devices
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