Neuro20 Technologies
Country not established
- Devices
- 6
What Neuro20 Technologies makes
Neuro20 Technologies manufactures the Neuro20 Pro System, a device designed for neuromodulation applications in clinical settings, targeting specific neurological conditions through electrical stimulation.
The Neuro20 Pro System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Neuro20 Pro System Ref K223797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuro20 Technologies have in the registry?
The registry currently lists 6 devices for Neuro20 Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro20 Technologies's devices?
Among its 6 most recently registered devices, Neuro20 Technologies 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 Neuro20 Technologies's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Neuro20 Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuro20 Technologies in the registry?
The most recently registered devices listed for Neuro20 Technologies include Neuro20 PRO Control Box N20-PRO-CB, Neuro20 PRO System N20-PRO-SYS-1:1, Neuro20 PRO System N20-PRO-SYS-1:2 and Neuro20 PRO System N20-PRO-SYS-1:4.