Brainbase Corporation
Country not established
- Devices
- 3
What Brainbase Corporation makes
Brainbase Corporation makes MYTIS ARROW XXXX, BETA-POWDER, ARROWBONE-A, and ARROWBONE-B.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Mytis Arrow Xxxx Ref K052254
510(k) 510(k)Beta-Powder Ref K063236
510(k) 510(k)Arrowbone-A, Arrowbone-B Ref K083372
510(k) 510(k)
Frequently asked questions
How many devices does Brainbase Corporation have in the registry?
The registry currently lists 3 devices for Brainbase Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brainbase Corporation's devices?
Among its 3 most recently registered devices, Brainbase Corporation has devices listed in FDA 510(k) (3 devices).
What risk classes do Brainbase Corporation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Brainbase Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brainbase Corporation in the registry?
The most recently registered devices listed for Brainbase Corporation include MYTIS ARROW XXXX, BETA-POWDER and ARROWBONE-A, ARROWBONE-B.