Coors Biomedical Co.
Coors Biomedical Co. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1986.
Top product codes for Coors Biomedical Co.
Recent clearances by Coors Biomedical Co.
- K863176 — ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+
- K862324 — OSTEOGRAF/AR AND OSTEOGRAF/AR+
- K862061 — OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40
- K861083 — OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESH
- K861084 — OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH
- K852742 — OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40
- K810822 — DENTAL PORCELAIN POWDER
Data sourced from openFDA. This site is unofficial and independent of the FDA.