Not currently registered with FDA under this name

Pro-Den Systems, Inc.

Vancouver, WA, United States. Named as applicant on 2 dental 510(k) clearances between 1993 and 1995. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21993–1995
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Pro-Den Systems, Inc. as the applicant.

Decided	510(k)	Device	Device type
21 Sep 1995	K954061	POLY-LITE MODEL 1000	EBZ Ultraviolet Activator for Polymerization
10 Sep 1993	K922942	PRO-SCOPE MODEL # PS-4000	EIA Operative Dental Unit

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.