Medical Device Manufacturer · US , Washington , DC

Anaxdent GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Anaxdent GmbH Dental ✕

2 devices

1-2 of 2

Cleared Jan 26, 2012

ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT...

Cleared Oct 30, 2002

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026