Forest Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Forest Devices, Inc. makes
Forest Devices, Inc. makes the SignalNED System (Model RE), a medical device designed for neurological monitoring.
The SignalNED System (Model RE) is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
SignalNED System (Model RE) Ref K251726
Regimes: 510(k) Registry: 510(k)SignalNED System (Model RE) Ref K242306
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Forest Devices, Inc. have in the registry?
The registry currently lists 2 devices for Forest Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Forest Devices, Inc.'s devices?
Among its 2 most recently registered devices, Forest Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Forest Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Forest Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Forest Devices, Inc. in the registry?
The most recently registered devices listed for Forest Devices, Inc. include SignalNED System (Model RE).