Anaxdent GmbH is one of 24165 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anaxdent GmbH - FDA 510(k) Cleared Devices
Recent clearances: ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A, NEW OUTLINE
2
Total
2
Cleared
0
Denied
Anaxdent GmbH has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 2002 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Anaxdent GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anaxdent GmbH
2 devices