Bauerfeind AG

FDA Regulatory Profile

Bauerfeind AG appears in FDA public data with 0 recalls, 2 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 26, 2013.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K123921BODYTRONIC 200April 26, 2013
K111662VENOTRAIN CURAFLOWOctober 4, 2011