Zirkonzahn GmbH is one of 18437 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, PRETTAU ANTERIOR T0, ZIRKONZAHN ICE
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.
510(k) submissions have been managed by Tuv Rheinland Italia S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Zirkonzahn GmbH
3 devices