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FDA 510(k) Applications Submitted by CDB Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091702
06/10/2009
CDB FLIP-SIDE-CLIP BRACKET
CDB CORPORATION
K080906
04/01/2008
CDB CLIP
CDB CORPORATION
K210613
03/01/2021
HIT Clear Aligner
CDB Corporation
K212173
07/12/2021
HDH Treatment Planning System
CDB Corporation
K191823
07/08/2019
Clear-Aligners
CDB Corporation
K160957
04/05/2016
CDB Self Ligating Bracket 8F
CDB CORPORATION
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