Medical Device Manufacturer · AT , Burmoos

W&H Dentalwerk Buermoss GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - W&H Dentalwerk Buermoss GmbH Dental ✕

2 devices

1-2 of 2

Cleared Jul 14, 2023

Proxeo ULTRA (PB-510, PB-520 and PB-530)

Cleared May 26, 2022

AMADEO, M-UK1015 (incl. attachments and accessories)