Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in South KoreaLabelled 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 13, 2026, FDA's public records list Dio Corporation and its 1 subsidiaries with 22 510(k) clearances. The most recent is a 510(k) clearance dated Aug 18, 2023: Eco Abutment, Multiunit Abutment.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Dio Corporation and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Aug 18, 2023 | Eco Abutment, Multiunit AbutmentK220253 · NHA | 510(k) clearances |
| Mar 23, 2021 | DIOnavi-Denture02K210828 · EBI | 510(k) clearances |
| Oct 22, 2020 | DIOnavi-DentureK193623 · EBI | 510(k) clearances |
| May 18, 2020 | UF(II) Bar holder abutmentK193404 · NHA | 510(k) clearances |
| Feb 21, 2020 | UCLA CCM AbutmentK192263 · NHA | 510(k) clearances |
| Sep 30, 2019 | UF(II) Anatomic abutmentK190048 · NHA | 510(k) clearances |
| Dec 21, 2018 | DIO CAD/CAM AbutmentK181037 · NHA | 510(k) clearances |
| Dec 14, 2018 | UV Active Implant SystemK182194 · DZE | 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
