Not currently registered with FDA under this name

U.S. Apatite Corp.

Canoga Park, CA, United States. Named as applicant on 2 dental 510(k) clearances between 1988 and 1988. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21988–1988
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names U.S. Apatite Corp. as the applicant.

Decided	510(k)	Device	Device type
5 Dec 1988	K883761	IONODENT II (6 VOLTS)	EFW Manual Toothbrush
19 Jul 1988	K874443	IONODENT (TOOTHBRUSH)	EFW Manual Toothbrush

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.