Home / Companies / Zimmer Medizinsystems GmbH

Zimmer Medizinsystems GmbH

FDA Regulatory Profile

Zimmer Medizinsystems GmbH appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 24, 2014.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K141564OPTON PROOctober 24, 2014
K121059SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIMAugust 7, 2012

FDA data resources