Not currently registered with FDA under this name

Biomedevice , Ltd.

Laguna Hills, CA, United States. Named as applicant on 1 dental 510(k) clearance between 2007 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12007–2007
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Biomedevice , Ltd. as the applicant.

Decided	510(k)	Device	Device type
5 Nov 2007	K072082	GUMEASE DENTAL MOUTHPIECE	KKO Fluid-Filled Teething Ring

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.