Medical Device Manufacturer · DE , Bietigheim-Bissingen

Duerr Dental AG - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2016

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Duerr Dental AG Dental ✕

1 devices

1-1 of 1

Cleared Nov 22, 2017

CamX Triton HD Proxi Head