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 13, 2026, FDA's public records list Orthomatrix with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 2001: CANNULATED PLUS SCREW SYSTEM.
| Date | Record | Source |
|---|---|---|
| Aug 1, 2001 | CANNULATED PLUS SCREW SYSTEMK010738 · HWC | 510(k) clearances |
| Dec 13, 2000 | ORTHOMATRIX, INC. CERCLAGE SYSTEMK001254 · JDQ | 510(k) clearances |
| Mar 10, 2000 | MAGELLAN HUMERAL INTRAMEDULLARY NAILK992856 · HSB | 510(k) clearances |
| Mar 10, 2000 | MAGELLAN TIBIAL INTRAMEDULLARY NAILK992850 · HSB | 510(k) clearances |
| Oct 21, 1985 | HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTIK852766 · LYC | 510(k) clearances |
| Sep 23, 1985 | HA-2000 HYDROXYLAPATITEK852765 · LYC | 510(k) clearances |
| May 21, 1985 | HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATIONK851367 · DZE | 510(k) clearances |
| Aug 9, 1984 | RIDGEMATRIX 20/40 MESH, PERIOMATRIXK842163 · LYC | 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
