Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Creodent Prosthetics, Ltd. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 2, 2022: CreoDent Solidex Customized Abutment and Screw.
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.
| Dec 2, 2022 | CreoDent Solidex Customized Abutment and ScrewK220390 · NHA | 510(k) clearances |
| Oct 13, 2022 | CREOKORREKT AlignersK211427 · NXC | 510(k) clearances |
| Apr 2, 2021 | CreoDent Solidex Customized AbutmentK202909 · NHA | 510(k) clearances |
| Dec 16, 2020 | CreoDent Solidex Customized Abutment and ScrewK202095 · NHA | 510(k) clearances |
| Jul 18, 2017 | CreoDent Solidex Customized Abutment and ScrewK170100 · NHA | 510(k) clearances |
| May 8, 2017 | CreoDent Solidex Customized AbutmentK162734 · NHA | 510(k) clearances |
| Sep 29, 2016 | CreoDent Solidex Custom AbutmentK160436 · NHA | 510(k) clearances |
| Jun 4, 2015 | CreoDent Solidex Customized AbutmentK150012 · NHA | 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
