Amann Girrbach AG

FDA Regulatory Profile

Amann Girrbach AG appears in FDA public data with 0 recalls, 4 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 29, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260918Zolid LunarisJune 29, 2026
K191836Ceramill A-SplintDecember 20, 2019
K191843Ceramill A-TempOctober 4, 2019
K171876Ceramill Zolid HT+ whiteSeptember 20, 2017