Not currently registered with FDA under this name

Wykle Research, Inc.

Carson City, NV, United States. Named as applicant on 3 dental 510(k) clearances between 1991 and 1995. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31991–1995
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Wykle Research, Inc. as the applicant.

Decided	510(k)	Device	Device type
25 Aug 1995	K952670	CUPRALLOY	EJJ Amalgam Alloy
10 Sep 1993	K921571	1ST IMPRESSION	ELW Impression Material
15 Mar 1991	K910632	ACCU-MIX AMALGAMATOR	EFD Ac-Powered Dental Amalgamator

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.