Not currently registered with FDA under this name

Silmet U.S.A. Corp.

North Miami Beach, FL, United States. Named as applicant on 1 dental 510(k) clearance between 1994 and 1994. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11994–1994
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Silmet U.S.A. Corp. as the applicant.

Decided	510(k)	Device	Device type
26 Jan 1994	K933766	HIGH-Q-BOND	EBF Resin Tooth Shade Material

Some of these clearances are listed with FDA today by another company: Premier Dental Products Company (1), Inter-Med, Inc. (1), B.J.M. Laboratories Ltd (1).

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.