Not currently registered with FDA under this name

Healex Products, Inc.

Providence, RI, United States. Named as applicant on 3 dental 510(k) clearances between 1996 and 2003. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31996–2003
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

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

Decided	510(k)	Device	Device type
5 Jun 2003	K030727	POTASSIUM NITRATE/ZINC OXIDE EUGENOL TEMPORARY DENTAL CEMENT	EMA Dental Cement
18 Jul 1996	K961457	SUBLIMINATOR	EJI Cartridge Syringe
25 Apr 1996	K954976	POTASSIUM NITRATE ZINC OXIDE EUGENOL TEMP CEMENT (MODIFICATION)	EBG Resin Temporary Crown and Bridge

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.