Company ยท US
Coors Biomedical Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1986. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 26, 1986 | K863176 | ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+ Coors Biomedical Co. | LYC |
| Aug 15, 1986 | K862324 | OSTEOGRAF/AR AND OSTEOGRAF/AR+ Coors Biomedical Co. | LYC |
| Jul 29, 1986 | K862061 | OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40 Coors Biomedical Co. | LYC |
| Apr 30, 1986 | K861084 | OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH Coors Biomedical Co. | LYC |
| Apr 30, 1986 | K861083 | OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESH Coors Biomedical Co. | LYC |
| Sep 26, 1985 | K852742 | OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 Coors Biomedical Co. | LYC |
| Apr 21, 1981 | K810822 | DENTAL PORCELAIN POWDER Coors Biomedical Co. | EIH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||