Not currently registered with FDA under this name

G-Ortho Lab

Honolulu, HI, United States. Named as applicant on 1 dental 510(k) clearance between 1990 and 1990. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11990–1990
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names G-Ortho Lab as the applicant.

Decided	510(k)	Device	Device type
19 Sep 1990	K902790	NAPA	LQZ Jaw Repositioning Device

Some of these clearances are listed with FDA today by another company: Great Lakes Dental Technologies, Ltd. (1).

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.