Columbus Dental Mfg. Co.

Columbus Dental Mfg. Co. holds 11 FDA 510(k) medical device clearances, first cleared 1983, most recent 1988.

Top product codes for Columbus Dental Mfg. Co.

EBF — Dental4 devices
EGD — Dental3 devices
ELW — Dental2 devices
EHZ — Dental1 device
EIE — Dental1 device

Recent clearances by Columbus Dental Mfg. Co.

K880754 — DRI-CLAVE LIQUID KLEENZALLCode EHZ·1988-05-12
K880607 — UTILITY WAX STRIPS, SPEARMINTCode EGD·1988-03-31
K880606 — UTILITY WAX STRIPS, CINNAMONCode EGD·1988-03-24
K872243 — PEKALUX(TM)Code EBF·1987-07-07
K871164 — GLUMA(TM) BONDING SYSTEMCode EBF·1987-07-02
K872272 — PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYSCode EBF·1987-07-02
K871165 — LUMIFOR(TM) COMPOSITECode EBF·1987-04-03
K863816 — IVORY PREMIUM RUBBER DAMCode EIE·1986-10-27
K863758 — ORTHO-BITE WAX WAFERCode EGD·1986-10-07
K860855 — SHUR GEL 4Code ELW·1986-06-16
K830083 — SHUR GELCode ELW·1983-02-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.