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BrainMaster Technologies, Inc.

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000008908 FEI 3002757680

BrainMaster Technologies, Inc. is a medical device manufacturer based in the United States, with 6 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (FDA Class II; EU Class IIa) as of 13 Nov 2026.

Devices
6
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • EUDAMED 5
  • FDA GUDID 4
  • FDA 510(k) 2

A device listed in two registries counts in both.

Device classes
  • FDA Class II 5
  • EU Class IIa 1
Top EMDN categories
Identifiers
  • EUDAMED SRN US-MF-000008908
  • FDA FEI 3002757680
  • DUNS 008607256

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What BrainMaster Technologies, Inc. makes

BrainMaster Technologies, Inc. manufactures electroencephalograph (EEG) systems, including devices for clinical EEG monitoring, quantitative EEG (qEEG) analysis, and neurofeedback applications. Examples include continuous recording systems like the Discovery 24 and Discovery models, as well as software tools such as qEEG-Pro and the Atlantis platform for 3D brain imaging.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

  • BrainAvatar Ref 533-145A

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Discovery Discovery 20

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • Discovery Discovery 24

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

  • Atlantis Atlantis 2eb+

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II

  • Discovery 24 Ref K150498

    Active Regimes: CE MDR 510(k) Registry: EUDAMED510(k)GUDID Class:II

  • qEEG-Pro Ref K171414

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000008908
FDA FEI number
3002757680
DUNS number
008607256
EUDAMED status
Active
EUDAMED registered name
BrainMaster Technologies, Inc.
Registered address
195, Willis Street, 44146, Bedford, United States
Phone
440 232-6000
PRRC contact
Thomas Collura(public in EUDAMED)

From the company website

Read 18 Oct 2026

BrainMaster makes the most cutting edge Clinical EEG, 3D Brain Imaging, QEEG and Neurofeedback Equipment and Software on the market.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does BrainMaster Technologies, Inc. have in the registry?

The registry currently lists 6 devices for BrainMaster Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list BrainMaster Technologies, Inc.'s devices?

Among its 6 most recently registered devices, BrainMaster Technologies, Inc. has devices listed in EUDAMED (5 devices), FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do BrainMaster Technologies, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for BrainMaster Technologies, Inc.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from BrainMaster Technologies, Inc. in the registry?

The most recently registered devices listed for BrainMaster Technologies, Inc. include BrainAvatar, Discovery Discovery 20, Discovery Discovery 24 and Atlantis Atlantis 2eb+.

Generated automatically from registry data and not verified by a human reviewer.