Vita Zahnfabrik GmbH H Rauter & CO

FDA Regulatory Profile

Vita Zahnfabrik GmbH H Rauter & CO appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 22, 2021.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K211854VITA Akzent LCNovember 22, 2021
K193434VITA LUMEX ACJuly 21, 2020
K193436VITA AmbriaMay 14, 2020