Wada, Inc.
Country not established
- Devices
- 1
What Wada, Inc. makes
Wada, Inc. manufactures the POTENS +, a device designed for measuring and analyzing electrical activity in the brain during surgical procedures, such as epilepsy evaluations.
The POTENS + 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
Potens + Ref K033137
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wada, Inc. have in the registry?
The registry currently lists 1 device for Wada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wada, Inc.'s devices?
Among its 1 most recently registered device, Wada, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wada, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wada, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wada, Inc. in the registry?
The most recently registered devices listed for Wada, Inc. include POTENS +.