Not currently registered with FDA under this name

Udent, Inc.

Pomona, CA, United States. Named as applicant on 1 dental 510(k) clearance between 2002 and 2002. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12002–2002
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Udent, Inc. as the applicant.

Decided	510(k)	Device	Device type
11 Feb 2002	K020009	BRACE EZE	EGD Intraoral Dental Wax

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.