Coors Biomedical Co. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Coors Biomedical Co. Dental ✕
7 devices
Cleared
Nov 26, 1986
ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+
Dental
100d
Cleared
Aug 15, 1986
OSTEOGRAF/AR AND OSTEOGRAF/AR+
Dental
57d
Cleared
Jul 29, 1986
OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40
Dental
60d
Cleared
Apr 30, 1986
OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESH
Dental
40d
Cleared
Apr 30, 1986
OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH
Dental
40d
Cleared
Sep 26, 1985
OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40
Dental
91d
Cleared
Apr 21, 1981
DENTAL PORCELAIN POWDER
Dental
28d