Home / Companies / Bionen S.A.S.

Bionen S.A.S.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K092973DISPOSABLE AND REUSABLE CONCENTRIC NEEDLES / DISPOSABLE AND REUSABLE MONOPOLAR NEEDLEOctober 7, 2010