Not currently registered with FDA under this name

A & F Products

Santa Ana, CA, United States. Named as applicant on 1 dental 510(k) clearance between 1991 and 1991. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11991–1991
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names A & F Products as the applicant.

Decided	510(k)	Device	Device type
15 May 1991	K911072	SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATOR	EHZ Oral Cavity Evacuator

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.