Goldsmith & Revere, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Goldsmith & Revere, Inc. makes
Goldsmith & Revere, Inc. manufactures dental alloys, including ultra-spherical amalgam alloys, dispersed phase alloys, and ternary alloys, as well as the Prince dental restoration system. These materials are designed for dental restorations and fillings, providing durable and biocompatible solutions for dentists.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. These products are intended for use in the United States, adhering to applicable medical device regulations.
Catalogue
Ultra Spherical Amalgam Alloy Ref K951865
Regimes: 510(k) Registry: 510(k)Dispersed Phase Alloy Ref K820617
Regimes: 510(k) Registry: 510(k)Prince Ref K933309
Regimes: 510(k) Registry: 510(k)Goldsmith & Revere Tenary Alloy Ref K821222
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Goldsmith & Revere, Inc. have in the registry?
The registry currently lists 4 devices for Goldsmith & Revere, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Goldsmith & Revere, Inc.'s devices?
Among its 4 most recently registered devices, Goldsmith & Revere, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Goldsmith & Revere, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Goldsmith & Revere, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Goldsmith & Revere, Inc. in the registry?
The most recently registered devices listed for Goldsmith & Revere, Inc. include ULTRA SPHERICAL AMALGAM ALLOY, DISPERSED PHASE ALLOY, PRINCE and GOLDSMITH & REVERE TENARY ALLOY.