Brain Tunnelgenix Technologies Corp
Country not established
- Devices
- 1
What Brain Tunnelgenix Technologies Corp makes
Brain Tunnelgenix Technologies Corp manufactures the ABREU Model 700, a medical device designed for neurostimulation or neuromodulation applications targeting neurological conditions.
The company’s portfolio is regulated under FDA Class II devices, with the ABREU Model 700 authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Abreu, Model 700 Ref K100843
510(k) 510(k)
Frequently asked questions
How many devices does Brain Tunnelgenix Technologies Corp have in the registry?
The registry currently lists 1 device for Brain Tunnelgenix Technologies Corp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brain Tunnelgenix Technologies Corp's devices?
Among its 1 most recently registered device, Brain Tunnelgenix Technologies Corp has devices listed in FDA 510(k) (1 device).
What risk classes do Brain Tunnelgenix Technologies Corp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Brain Tunnelgenix Technologies Corp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brain Tunnelgenix Technologies Corp in the registry?
The most recently registered devices listed for Brain Tunnelgenix Technologies Corp include ABREU, MODEL 700.