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VBM Medizintechnik GmbH

FDA Regulatory Profile

VBM Medizintechnik GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on October 30, 2020.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K200190ScalpelCricOctober 30, 2020
K112783MANUJET IIIDecember 22, 2011
K955461TRANSTRACHEAL CATHETER (ACC. RAVUSSIN).March 19, 1997

FDA data resources