Zirkonzahn GmbH

FDA Regulatory Profile

Zirkonzahn GmbH appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 5, 2023.

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Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232691PolibondSep 5, 2023
K213722ICE Ceramics, ICE Stains, FrescoDec 14, 2022
K203765ZIRKONZAHN.Implant-Planner, ZIRKONZAHN.Implant-Planner Practice, CAD/CAM STL Converter, CAD/CAM…Jul 20, 2021
K200676ABRO 1, RESITON GINGIVA, PRIME and THERAPON TRANSPAJul 8, 2020
K190518Color Liquid, Vita LiquidNov 22, 2019
K183304Prettau, ICE, Z-White zirconia blanksApr 4, 2019
K180562TEMP BASIC, TEMP PREMIUM, TEMP PREMIUM FLEXIBLE, MULTISTRATUM FLEXIBLE, THERAPON, TRY-IN, BURNOUT…Jun 28, 2018
K181484Tecno Med, Tecno Med Mineral, Tecno Med Mineral Dentine, Tecno Med Mineral TissueJun 18, 2018
K151490PRETTAU ANTERIOR T0Oct 8, 2015
K132230ICE ZIRKON TRANSLUZENTNov 5, 2014
K061851ZIRKONZAHN ICESep 29, 2006