Medical Device Manufacturer · DE , Pforzheim

Bernhard F?rster GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
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Cleared
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Denied

Bernhard F?rster GmbH has 1 FDA 510(k) cleared medical devices. Based in Pforzheim, DE.

Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Bernhard F?rster GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Bernhard Förster GmbH as regulatory consultant.

FDA 510(k) Regulatory Record - Bernhard F?rster GmbH
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