Aeon Astron Europe B.V.

FDA Regulatory Profile

Aeon Astron Europe B.V. appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 2, 2018.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K173223ologen Collagen MatrixMarch 2, 2018
K112568AONGEN DENTAL COLLAGEN MATRIXMarch 1, 2012
K080868AONGEN COLLAGEN MATRIXMay 14, 2009