MIND MEDIA

FDA Device Registration & Listing · ROERMOND-HERTEN Limburg, NL · Registration 3005024415

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005024415
FEI Number
3005024415
Entity Name
MIND MEDIA
City/State/Country
ROERMOND-HERTEN Limburg, NL
Establishment Address
Boven de Wolfskuil 3B 3, ROERMOND-HERTEN Limburg NL6049-LX, NL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MIND MEDIA GROUP (NeuroLOGX B.V.) (Owner Number: 9070318)
Owner / Operator Contact Address
Boven de Wolfskuil 3B 3, --, ROERMOND-HERTEN, NL-LI NL-6049LX, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mind Media NeXus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2005-02-14

Official Correspondent

ERWIN HARTZUIKER

US Agent Details

Wes Center Business: NEUROFEEDBACK SUPPLY & EQUIPMENT OF TEXAS, LLC Email: wes@nexusbiotrace.com Phone: (817) 7136950

Related Public Records

Same Entity

MIND MEDIA GROUP (NeuroLOGX B.V.)
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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005024415. Last updated year: 2026. Please use registration number 3005024415 when referencing this establishment in official correspondence.
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