Home / Companies / Storz Medical AG

Storz Medical AG

FDA Regulatory Profile

Storz Medical AG appears in FDA public data with 0 recalls, 3 510(k) clearances, 3 FDA inspections, and 2 compliance actions on record. Its most recent 510(k) clearance was granted on May 3, 2021.

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

FDA data resources