Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Ortho Tec with 22 510(k) clearances. The most recent is a 510(k) clearance dated May 3, 2004: EOVIA CALCIUM PHOSPHATE CERAMIC.
| Date | Record | Source |
|---|---|---|
| May 3, 2004 | EOVIA CALCIUM PHOSPHATE CERAMICK040514 · MQV | 510(k) clearances |
| Mar 12, 2004 | MODIFICATION TO ORIA TOP CLIP SYSTEMK040346 · MNI | 510(k) clearances |
| Nov 20, 2003 | ORIA SPINAL SYSTEM, DOMINO AND TUBE CONNECTORSK030958 · MNI | 510(k) clearances |
| Oct 10, 2003 | ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01K031471 · KWP | 510(k) clearances |
| Aug 20, 2003 | MODIFICATION ORIA SPINAL SYSTEMK023884 · KWP | 510(k) clearances |
| Jun 27, 2003 | ORIA CLARISK023378 · MNH | 510(k) clearances |
| Jun 18, 2003 | ORIA SPINAL CLIP SYSTEM, SACRAL CONNECTOR, MODELS CA03 AND AO03K031452 · KWP | 510(k) clearances |
| Mar 20, 2003 | ORIA ZENITHK030500 · KWQ | 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
