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Storz Medical AG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
2

Recent 510(k) Clearances

K-NumberDeviceDate
K203710Storz Medical MAGNETOLITH Muscle StimulatorMay 3, 2021
K202112Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia HandpieceFebruary 21, 2021
K173692D-Actor 200 Vibration Massage SystemApril 13, 2018