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Biedermann Motech GmbH

FDA Regulatory Profile

Biedermann Motech GmbH appears in FDA public data with 0 recalls, 2 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 25, 1990.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K894184BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEMApril 25, 1990
K900138MOTECH TITANIUM SURGICAL MESHMarch 20, 1990

FDA data resources