NeuroCatch Inc
Country not established
NeuroCatch Inc is a medical device manufacturer, with 9 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 9
Registry facts
- Registries
- FDA GUDID 9
- Device classes
- FDA Class II 9
- Sites and related companies
- NeuroCatch Inc. Canada
- Identifiers
- DUNS 203694427
What NeuroCatch Inc makes
NeuroCatch Inc manufactures electroencephalograph (EEG) monitoring systems, including disposable EEG caps and a central processing platform designed for continuous or intermittent brainwave recording. The devices are intended for clinical use in detecting and analyzing neurological activity, such as seizures or epileptic events, in patients.
The company’s EEG-related products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 203694427
Sites
- NeuroCatch Inc. CAFEI 3013756694 0 devices
Frequently asked questions
How many devices does NeuroCatch Inc have in the registry?
The registry currently lists 9 devices for NeuroCatch Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list NeuroCatch Inc's devices?
Among its 9 most recently registered devices, NeuroCatch Inc has devices listed in FDA GUDID (9 devices).
What risk classes do NeuroCatch Inc's devices fall under?
Among its 9 most recently registered devices, the classes recorded for NeuroCatch Inc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NeuroCatch Inc in the registry?
The most recently registered devices listed for NeuroCatch Inc include NeuroCatch EEG Cap 2.0, NeuroCatch Platform 2.0 and NeuroCatch EPiO 2.0.