Medical Device Manufacturer · DE , Ettingen

Detax GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

Detax GmbH has 3 FDA 510(k) cleared medical devices. Based in Ettingen, DE.

Latest FDA clearance: Oct 2025. Active since 2022. Primary specialty: Dental.

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

Regulatory submissions have been managed by Aclivi, LLC and Regulatory Technology Services, LLC.

FDA 510(k) Regulatory Record - Detax GmbH
3 devices
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All3 Dental 3