Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list CDB Corporation with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 25, 2022: HDH Treatment Planning System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jan 25, 2022 | HDH Treatment Planning SystemK212173 · PNN | 510(k) clearances |
| Jun 4, 2021 | HIT Clear AlignerK210613 · NXC | 510(k) clearances |
| Dec 20, 2019 | Clear-AlignersK191823 · NXC | 510(k) clearances |
| Sep 27, 2016 | CDB Self Ligating Bracket 8FK160957 · NJM | 510(k) clearances |
| Aug 7, 2009 | CDB FLIP-SIDE-CLIP BRACKETK091702 · NJM | 510(k) clearances |
| Oct 17, 2008 | CDB CLIPK080906 · NJM | 510(k) clearances |
| Nov 21, 1997 | REFLECTIONSK973776 · DYW | 510(k) clearances |
| Feb 1, 1994 | REFLECTIONSK934881 · EJF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
