Cagenix, Inc.
Country not established
- Devices
- 6
What Cagenix, Inc. makes
Cagenix, Inc. manufactures custom-made dental implant suprastructures designed for permanent use, including resin artificial teeth. Their portfolio includes overdenture frameworks and bar attachments for stabilizing dental prosthetics, such as the AccuFrame 360 and BarZero systems.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) and UDI pathways. The company’s products are listed in the FDA’s regulatory databases, and the manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Accuframe Ref K081157
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 030868250
- [email protected]
- Phone
- 901-763-3784
Frequently asked questions
How many devices does Cagenix, Inc. have in the registry?
The registry currently lists 6 devices for Cagenix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cagenix, Inc.'s devices?
Among its 6 most recently registered devices, Cagenix, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cagenix, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Cagenix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cagenix, Inc. in the registry?
The most recently registered devices listed for Cagenix, Inc. include Cagenix AccuFrame Overdenture 1000-04, Cagenix BarZero 1000-05, Cagenix AccuFrame 360 1000-03 and Cagenix AccuFrame 1000-01.