Not currently registered with FDA under this name

Product Development Industries, Inc.

Tucson, AZ, United States. Named as applicant on 1 dental 510(k) clearance between 2000 and 2000. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12000–2000
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Product Development Industries, Inc. as the applicant.

Decided	510(k)	Device	Device type
25 Oct 2000	K002675	MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM	EJT Gold-Based Noble Metal Alloy

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.