# Columbus Dental Mfg. Co.

- Location (FDA's records): St. Louis, MO
- FDA decisions: 11 (1983–1988): 11 510(k) clearances
- Product codes: EBF (4), EGD (3), ELW (2), EHZ (1), EIE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K880754: Dri-Clave Liquid Kleenzall (May 12, 1988)
- K880607: Utility Wax Strips, Spearmint (Mar 31, 1988)
- K880606: Utility Wax Strips, Cinnamon (Mar 24, 1988)
- K872243: Pekalux (TM) (Jul 7, 1987)
- K872272: Pekalux/Gluma Light Cured Anterior Restorative Sys (Jul 2, 1987)
- K871164: Gluma (TM) Bonding System (Jul 2, 1987)
- K871165: Lumifor (TM) Composite (Apr 3, 1987)
- K863816: Ivory Premium Rubber Dam (Oct 27, 1986)

Source page: https://510kreport.com/company/columbus-dental-mfg