Medical Device Manufacturer · US , Mchenry , IL

Columbus Dental Mfg. Co. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1983

11

Total

11

Cleared

0

Denied

FDA 510(k) Regulatory Record - Columbus Dental Mfg. Co. Dental ✕

11 devices

1-11 of 11

Cleared May 12, 1988

DRI-CLAVE LIQUID KLEENZALL

Cleared Mar 31, 1988

UTILITY WAX STRIPS, SPEARMINT

Cleared Mar 24, 1988

UTILITY WAX STRIPS, CINNAMON

Cleared Jul 07, 1987

Cleared Jul 02, 1987

GLUMA(TM) BONDING SYSTEM

Cleared Jul 02, 1987

PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS

Cleared Apr 03, 1987

LUMIFOR(TM) COMPOSITE

Cleared Oct 27, 1986

IVORY PREMIUM RUBBER DAM

Cleared Oct 07, 1986

ORTHO-BITE WAX WAFER

Cleared Jun 16, 1986

Cleared Feb 07, 1983