W&H Dentalwerk Buermoss GmbH is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
W&H Dentalwerk Buermoss GmbH - FDA 510(k) Cleared Devices
Recent clearances: Proxeo ULTRA (PB-510, PB-520 and PB-530), AMADEO, M-UK1015 (incl. attachments and accessories)
2
Total
2
Cleared
0
Denied
W&H Dentalwerk Buermoss GmbH has 2 FDA 510(k) cleared medical devices. Based in Burmoos, AT.
Last cleared in 2023. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by W&H Dentalwerk Buermoss GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - W&H Dentalwerk Buermoss GmbH
2 devices