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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