Not currently registered with FDA under this name
Goldsmith & Revere, Inc.
Englewood, NJ, United States. Named as applicant on 4 dental 510(k) clearances between 1982 and 1995. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41982–1995
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Goldsmith & Revere, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 25 May 1995 | K951865 | ULTRA SPHERICAL AMALGAM ALLOY | EJJ Amalgam Alloy |
| 1 Oct 1993 | K933309 | PRINCE | EJJ Amalgam Alloy |
| 24 May 1982 | K821222 | GOLDSMITH & REVERE TENARY ALLOY | EJJ Amalgam Alloy |
| 25 Mar 1982 | K820617 | DISPERSED PHASE ALLOY | EJJ Amalgam Alloy |
Some of these clearances are listed with FDA today by another company: DMG America, L.L.C. (3).
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.