Not currently registered with FDA under this name

Western M/D, Inc.

Burlingame, CA, United States. Named as applicant on 2 dental 510(k) clearances between 1991 and 1994. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21991–1994
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Western M/D, Inc. as the applicant.

Decided	510(k)	Device	Device type
7 Mar 1994	K931772	SURETIP SYRINGE TIP COVER	ECB Air and/or Water Syringe Unit
17 Jul 1991	K911214	NUTIP (TM) SYRINGE SHIELD	EKJ Operative Burnisher

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.