Not currently registered with FDA under this name
Columbus Dental Mfg. Co.
St. Louis, MO, United States. Named as applicant on 11 dental 510(k) clearances between 1983 and 1988. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 111983–1988
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Columbus Dental Mfg. Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 12 May 1988 | K880754 | DRI-CLAVE LIQUID KLEENZALL | EHZ Oral Cavity Evacuator |
| 31 Mar 1988 | K880607 | UTILITY WAX STRIPS, SPEARMINT | EGD Intraoral Dental Wax |
| 24 Mar 1988 | K880606 | UTILITY WAX STRIPS, CINNAMON | EGD Intraoral Dental Wax |
| 7 Jul 1987 | K872243 | PEKALUX(TM) | EBF Resin Tooth Shade Material |
| 2 Jul 1987 | K872272 | PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS | EBF Resin Tooth Shade Material |
| 2 Jul 1987 | K871164 | GLUMA(TM) BONDING SYSTEM | EBF Resin Tooth Shade Material |
| 3 Apr 1987 | K871165 | LUMIFOR(TM) COMPOSITE | EBF Resin Tooth Shade Material |
| 27 Oct 1986 | K863816 | IVORY PREMIUM RUBBER DAM | EIE Rubber Dam |
| 7 Oct 1986 | K863758 | ORTHO-BITE WAX WAFER | EGD Intraoral Dental Wax |
| 16 Jun 1986 | K860855 | SHUR GEL 4 | ELW Impression Material |
| 7 Feb 1983 | K830083 | SHUR GEL | ELW Impression Material |
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.