Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1531052

FEI Number

3002757680

Entity Name

BRAINMASTER TECHNOLOGIES, INC.

City/State/Country

Bedford, OH, US

Establishment Address

195 Willis Street Suite No. 3, Bedford, OH 44146, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

BRAINMASTER TECHNOLOGIES, INC. (Owner Number: 9038365)

Owner / Operator Contact Address

195 Willis Street Suite #3, --, Bedford, OH 44146, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K171414

PMA Number

N/A

All Registered Proprietary Names

Discovery Atlantis 2E Freedom qEEG-Pro Meant

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	1999-06-29
OLU	Normalizing Quantitative Electroencephalograph Software	Neurology	Class 2	882.1400	2024-04-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BRAINMASTER TECHNOLOGIES, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

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3038620647	KISO EHF	Reykjavik, IS
3005196642	HARMONIC ENERGETIC TECHNOLOGIES, LLC	Liverpool, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1531052. Last updated year: 2026. Please use registration number 1531052 when referencing this establishment in official correspondence.