Neuroone, Inc.
Country not established
- Devices
- 1
What Neuroone, Inc. makes
Neuroone, Inc. manufactures the NeuroOne Cortical Electrode, a device designed for recording and stimulating the brain’s cortical surface to support neurological research and clinical monitoring.
The NeuroOne Cortical Electrode is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
NeuroOne Cortical Electrode Ref K192764
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuroone, Inc. have in the registry?
The registry currently lists 1 device for Neuroone, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuroone, Inc.'s devices?
Among its 1 most recently registered device, Neuroone, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuroone, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuroone, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuroone, Inc. in the registry?
The most recently registered devices listed for Neuroone, Inc. include NeuroOne Cortical Electrode.