Medical Device Manufacturer · AT , Buermoos

W&H Dentalwerk B?rmoos GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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Cleared
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Denied

W&H Dentalwerk B?rmoos GmbH has 1 FDA 510(k) cleared medical devices. Based in Buermoos, AT.

Latest FDA clearance: Feb 2025. 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
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