Not currently registered with FDA under this name

Syntex Dental Products, Inc.

Mchenry, IL, United States. Named as applicant on 3 dental 510(k) clearances between 1982 and 1983. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31982–1983
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Syntex Dental Products, Inc. as the applicant.

Decided	510(k)	Device	Device type
4 Oct 1983	K832378	VIBRATORY ENDODONTIC SYSTEM	EKQ Root Canal Endodontic Preparer
3 Dec 1982	K823230	STERILE WATER SYSTEM	EIA Operative Dental Unit
14 Sep 1982	K822610	PRECAPSULED DENTAL AMALGAM	DZS Amalgam Dental Capsule

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.