Not currently registered with FDA under this name

Metalor Technologies USA

North Attleborough, MA, United States. Named as applicant on 4 dental 510(k) clearances between 2001 and 2002. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 42001–2002
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Metalor Technologies USA as the applicant.

Decided	510(k)	Device	Device type
14 Feb 2002	K020062	XERAFIT	EJH Base Metal Alloy
22 Jan 2002	K013769	V-GNATHOS SUPRA	EJT Gold-Based Noble Metal Alloy
3 Jan 2002	K013506	YELLOW SPECIAL	EJT Gold-Based Noble Metal Alloy
19 Dec 2001	K013505	AUROFLUID PLUS	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.