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 15, 2026, FDA's public records list Coors Biomedical Co. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 26, 1986: ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+.
| Nov 26, 1986 | ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+K863176 · LYC | 510(k) clearances |
| Aug 15, 1986 | OSTEOGRAF/AR AND OSTEOGRAF/AR+K862324 · LYC | 510(k) clearances |
| Jul 29, 1986 | OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40K862061 · LYC | 510(k) clearances |
| Apr 30, 1986 | OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESHK861084 · LYC | 510(k) clearances |
| Apr 30, 1986 | OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESHK861083 · LYC | 510(k) clearances |
| Sep 26, 1985 | OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40K852742 · LYC | 510(k) clearances |
| Apr 21, 1981 | DENTAL PORCELAIN POWDERK810822 · EIH | 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
