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., part of Dio CorporationLabelled 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 Dio Department Dsi, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 30, 2008: SECURE IMPLANT SYSTEM (2.5/3.0MM).
| May 30, 2008 | SECURE IMPLANT SYSTEM (2.5/3.0MM)K080129 · DZE | 510(k) clearances |
| May 16, 2008 | DIO BIOTITE-H IMPLANT SYSTEMK073070 · DZE | 510(k) clearances |
| May 14, 2008 | SM-EXTRA WIDE (RBM) IMPLANT SYSTEMK080128 · DZE | 510(k) clearances |
| Apr 15, 2008 | DIO IMPLANT SYSTEMK070570 · DZE | 510(k) clearances |
| Apr 11, 2008 | DIO PROTEM IMPLANT SYSTEMK080126 · DZE | 510(k) clearances |
| Nov 8, 2007 | SM INTERNAL./EXTERNAL IMPLANT SYSTEMK070569 · DZE | 510(k) clearances |
| May 25, 2007 | DIO PROTEM IMPLANT SYSTEMK070568 · DZE | 510(k) clearances |
| Sep 1, 2006 | SM IMPLANT SYSTEMSK061797 · 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
