Facial Alveodental Implant Rehabilitation, Inc.
Country not established
- Devices
- 1
What Facial Alveodental Implant Rehabilitation, Inc. makes
Facial Alveodental Implant Rehabilitation, Inc. manufactures the FLEXIROOT, a dental implant designed for alveolar ridge rehabilitation, intended to restore function and aesthetics in patients requiring bone integration for single-tooth or multi-tooth replacements.
The FLEXIROOT is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Flexiroot Ref K852305
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Facial Alveodental Implant Rehabilitation, Inc. have in the registry?
The registry currently lists 1 device for Facial Alveodental Implant Rehabilitation, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Facial Alveodental Implant Rehabilitation, Inc.'s devices?
Among its 1 most recently registered device, Facial Alveodental Implant Rehabilitation, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Facial Alveodental Implant Rehabilitation, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Facial Alveodental Implant Rehabilitation, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Facial Alveodental Implant Rehabilitation, Inc. in the registry?
The most recently registered devices listed for Facial Alveodental Implant Rehabilitation, Inc. include FLEXIROOT.