FDA 510(k) Applications Submitted by Leah M Lehman
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| 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 |
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