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Vita Zahnfabrik H.Rauter GmbH & Co.

FDA Regulatory Profile

Vita Zahnfabrik H.Rauter GmbH & Co. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Feb 21, 2025

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances8Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K243940VITA YZ Multi TranslucentFeb 21, 2025
K180703VITA YZ ST and VITA YZ XTAug 1, 2018
K153645VITA ENAMIC Implant Solutions (IS)Jun 30, 2016
K152373VITA VM LC FlowDec 30, 2015
K132070VITA SUPRINITY(R)Jan 31, 2014
K122269ENAMICDec 13, 2012
K102128VITABLOCSAug 11, 2010
K090644VITABLOCS, MODEL VX55-****Mar 31, 2009

FDA data resources