Amann Girrbach AG is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Amann Girrbach AG - FDA 510(k) Cleared Devices
Recent clearances: Ceramill A-Splint, Ceramill A-Temp
3
Total
3
Cleared
0
Denied
Amann Girrbach AG has 3 FDA 510(k) cleared medical devices. Based in Koblach, AT.
Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Amann Girrbach AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Europe Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Amann Girrbach AG
3 devices