Brainmaster
Country not established
- Devices
- 1
What Brainmaster makes
Brainmaster designs and manufactures biofeedback devices, including the Brainmaster 2E Module paired with associated software for clinical use. These systems are intended to help users monitor and train physiological responses, such as brainwave activity, through real-time feedback.
The company’s biofeedback devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where Brainmaster is based.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Brainmaster have in the registry?
The registry currently lists 1 device for Brainmaster. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brainmaster's devices?
Among its 1 most recently registered device, Brainmaster has devices listed in FDA 510(k) (1 device).
What risk classes do Brainmaster's devices fall under?
Among its 1 most recently registered device, the classes recorded for Brainmaster's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brainmaster in the registry?
The most recently registered devices listed for Brainmaster include BRAINMASTER 2E MODULE AND SOFTWARE BIOFEEDBACK DEVICE.