W&H Dentalwerk B?rmoos GmbH is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
W&H Dentalwerk B?rmoos GmbH - FDA 510(k) Cleared Devices
Recent clearances: Synea Fusion Handpieces (Intensiv & Profin)
2
Total
2
Cleared
0
Denied
W&H Dentalwerk B?rmoos GmbH has 2 FDA 510(k) cleared medical devices. Based in Buermoos, AT.
Latest FDA clearance: Jul 2026. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by W&H Dentalwerk B?rmoos GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by W&H Dentalwerk Bürmoos GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - W&H Dentalwerk B?rmoos GmbH
2 devices