Zirkonzahn GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zirkonzahn GmbH - FDA 510(k) Cleared Devices
Recent clearances: TEMP BASIC, TEMP PREMIUM, TEMP PREMIUM FLEXIBLE, MULTISTRATUM FLEXIBLE, THERAPON, TRY-IN, BURNOUT, TRY-IN & BURNOUT
3
Total
3
Cleared
0
Denied
Zirkonzahn GmbH has 3 FDA 510(k) cleared medical devices. Based in Silver Creek, US.
Historical record: 3 cleared submissions from 2006 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Zirkonzahn GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zirkonzahn GmbH
3 devices