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 14, 2026, FDA's public records list O Co. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Dec 10, 2003: IMMEDIATE STABILIZING IMPLANT (ISI).
| Dec 10, 2003 | IMMEDIATE STABILIZING IMPLANT (ISI)K033392 · DZE | 510(k) clearances |
| Oct 9, 2002 | OCO DENTAL IMPLANT (5.0MM DIAMETER)K023336 · DZE | 510(k) clearances |
| May 22, 2002 | OCO DENTAL IMPLANTK021460 · NHA | 510(k) clearances |
| Apr 10, 2002 | IMMEDIATE STABILIZING DEVICE (ISD)K011524 · DZE | 510(k) clearances |
| Feb 1, 2001 | OCO DENTAL IMPLANTK010142 · DZE | 510(k) clearances |
| Jan 5, 1998 | O BUTMENT HS IMPLANTK973926 · DZE | 510(k) clearances |
| Nov 15, 1996 | O BUTMENT ET IMPLANTK961665 · DZE | 510(k) clearances |
| Sep 15, 1995 | DENTAL IMPLANT ENDOSSEOUSK950066 · 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
