Data / Medical devices / United States / Brainmaster Technologies, Inc.
Brainmaster Technologies, Inc.: FDA-registered device maker in Bedford, OH, United States, 2 510(k) clearances
Brainmaster Technologies, Inc. is registered with the FDA (registration 1531052) in Bedford, OH, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 1, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1531052
- FEI number
- 3002757680
- Address
- 195 Willis Street Suite No. 3, Bedford, OH, United States, 44146
- Owner or operator
- BRAINMASTER TECHNOLOGIES, INC. (9038365)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 29, 1999
- Registered through
- 2026
- Brand names listed
- 2E, Atlantis, Discovery, Discovery EEG, Freedom, Meant, qEEG-Pro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Biofeedback | HCC | 2 | Manufacturer | accessdata.fda.gov |
| Full-Montage Standard Electroencephalograph | GWQ | 2 | Manufacturer | accessdata.fda.gov |
| Normalizing Quantitative Electroencephalograph Software | OLU | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 1, 2018 | K171414 | qEEG-Pro | OLU | Substantially Equivalent | Brainmaster Technologies, Inc. | accessdata.fda.gov |
| January 26, 2016 | K150498 | Discovery 24 | GWQ | Substantially Equivalent | Brainmaster Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Biofeedback
- All makers of Full-Montage Standard Electroencephalograph
- All makers of Normalizing Quantitative Electroencephalograph Software
Updated July 1, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.