Braintech, Inc.
Country not established
- Devices
- 1
What Braintech, Inc. makes
Braintech, Inc. manufactures the Model SIX BEAM SYSTEM, a Class II medical device designed for neurostimulation or neuromodulation applications, likely targeting conditions such as chronic pain or neurological disorders.
The Model SIX BEAM SYSTEM is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Model Six Beam System Ref K811848
510(k) 510(k)
Frequently asked questions
How many devices does Braintech, Inc. have in the registry?
The registry currently lists 1 device for Braintech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Braintech, Inc.'s devices?
Among its 1 most recently registered device, Braintech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Braintech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Braintech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Braintech, Inc. in the registry?
The most recently registered devices listed for Braintech, Inc. include MODEL SIX BEAM SYSTEM.