American Dent-All, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What American Dent-All, Inc. makes
American Dent-All, Inc. manufactures dental casting systems, including the SUPREMCAST V and SUPREMCAST for precision metal restorations, as well as the FLEXICAST PRIME and FLEXICAST for flexible dental applications. The company also produces SUPERBOND, a dental adhesive used for bonding restorations to tooth structures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Supremcast V Ref K001383
Regimes: 510(k) Registry: 510(k)Supremcast Ref K011705
Regimes: 510(k) Registry: 510(k)Flexicast Prime Ref K011706
Regimes: 510(k) Registry: 510(k)Flexicast Ref K003509
Regimes: 510(k) Registry: 510(k)Superbond Ref K030161
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Dent-All, Inc. have in the registry?
The registry currently lists 5 devices for American Dent-All, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Dent-All, Inc.'s devices?
Among its 5 most recently registered devices, American Dent-All, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do American Dent-All, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Dent-All, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Dent-All, Inc. in the registry?
The most recently registered devices listed for American Dent-All, Inc. include SUPREMCAST V, SUPREMCAST, FLEXICAST PRIME and FLEXICAST.