R Tree Innovations
Country not established
- Devices
- 1
What R Tree Innovations makes
R Tree Innovations manufactures the EPICAGE Interbody Fusion Device, a spinal implant designed for intervertebral fusion procedures in the lumbar or cervical spine. This device is intended to provide structural support and promote bone growth between vertebrae, aiding in the stabilization of the spine during surgical interventions.
The company’s portfolio is regulated under Class II medical devices in the United States, with the EPICAGE Interbody Fusion Device authorised via the FDA’s 510(k) pathway. The device is listed in the FDA’s 510(k) database, adhering to regulatory requirements for spinal fusion implants. The manufacturer operates from the United States.
Catalogue
Epicage Interbody Fusion Device Ref K092901
510(k) 510(k)
Frequently asked questions
How many devices does R Tree Innovations have in the registry?
The registry currently lists 1 device for R Tree Innovations. Devices recorded under merged duplicate company entries are counted once.
Which registries list R Tree Innovations's devices?
Among its 1 most recently registered device, R Tree Innovations has devices listed in FDA 510(k) (1 device).
What risk classes do R Tree Innovations's devices fall under?
Among its 1 most recently registered device, the classes recorded for R Tree Innovations's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from R Tree Innovations in the registry?
The most recently registered devices listed for R Tree Innovations include EPICAGE INTERBODY FUSION DEVICE.