Medical Device Manufacturer · US , Washington , DC

Anaxdent GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Recent clearances: ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A, NEW OUTLINE

View 2 510(k) Devices ↓

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 . 176,325 total devices indexed.

Last updated: Sep 16, 2026