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 Denar Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 28, 1992: ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEM.
| Dec 28, 1992 | ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEMK925705 · IWY | 510(k) clearances |
| Dec 9, 1992 | COLLIMATOR LIGHT SOURCEK924759 · IZT | 510(k) clearances |
| Feb 10, 1989 | STERI-OSSK884845 · DZE | 510(k) clearances |
| Jan 13, 1989 | STERI-OSS HYDROXYAPATITE-COATED DENTAL IMPLANTK883373 · DZE | 510(k) clearances |
| Sep 23, 1985 | DENAR DENTAL IMPLANTK852802 · 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
