Zimmer Medizinsystems GmbH is one of 491 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Zimmer Medizinsystems GmbH - FDA 510(k) Cleared Devices
Recent clearances: OPTON PRO, SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIM
2
Total
2
Cleared
0
Denied
Zimmer Medizinsystems GmbH has 2 FDA 510(k) cleared medical devices. Based in Neu-Elm, DE.
Historical record: 2 cleared submissions from 2012 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Zimmer Medizinsystems GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zimmer Medizinsystems GmbH
2 devices