Coors Biomedical Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coors Biomedical Co. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
Coors Biomedical Co. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1986. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Coors Biomedical Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coors Biomedical Co.
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