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Cdb Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K212173HDH Treatment Planning SystemJanuary 25, 2022
K210613HIT Clear AlignerJune 4, 2021
K191823Clear-AlignersDecember 20, 2019
K160957CDB Self Ligating Bracket 8FSeptember 27, 2016
K091702CDB FLIP-SIDE-CLIP BRACKETAugust 7, 2009
K080906CDB CLIPOctober 17, 2008