Columbus Dental Mfg. Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Columbus Dental Mfg. Co. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Columbus Dental Mfg. Co. has 11 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1983 to 1988.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Columbus Dental Mfg. Co.
11 devices
Cleared
May 12, 1988
DRI-CLAVE LIQUID KLEENZALL
Dental
77d
Cleared
Mar 31, 1988
UTILITY WAX STRIPS, SPEARMINT
Dental
48d
Cleared
Mar 24, 1988
UTILITY WAX STRIPS, CINNAMON
Dental
41d
Cleared
Jul 07, 1987
PEKALUX(TM)
Dental
26d
Cleared
Jul 02, 1987
GLUMA(TM) BONDING SYSTEM
Dental
100d
Cleared
Jul 02, 1987
PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS
Dental
20d
Cleared
Apr 03, 1987
LUMIFOR(TM) COMPOSITE
Dental
10d
Cleared
Oct 27, 1986
IVORY PREMIUM RUBBER DAM
Dental
27d
Cleared
Oct 07, 1986
ORTHO-BITE WAX WAFER
Dental
12d
Cleared
Jun 16, 1986
SHUR GEL 4
Dental
101d
Cleared
Feb 07, 1983
SHUR GEL
Dental
27d