Brainways, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 1
What Brainways, Ltd. makes
Brainways, Ltd. manufactures the Brainsway Deep Transcranial Magnetic Stimulation (DTMS) System, a device designed for non-invasive brain stimulation therapy.
The company’s portfolio is regulated under Class II devices in the U.S. and is listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- De Novo 510(k)
Frequently asked questions
How many devices does Brainways, Ltd. have in the registry?
The registry currently lists 1 device for Brainways, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brainways, Ltd.'s devices?
Among its 1 most recently registered device, Brainways, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Brainways, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Brainways, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brainways, Ltd. in the registry?
The most recently registered devices listed for Brainways, Ltd. include Brainsway Deep Transcranial Magnetic Stimulation (DTMS) System.