Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013755083

FEI Number

3013755083

Entity Name

WHITE DOVE GLOBAL MARKETING, LTD

City/State/Country

Commerce Township, MI, US

Establishment Address

2655 E. Oakley Park Dr., Suite 105, Commerce Township, MI 48390, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

White Dove Global Marketing, Ltd (Owner Number: 10055328)

Owner / Operator Contact Address

2655 E. Oakley Park Dr., Suite 104, Commerce Twp, MI 48390, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

QUEX ED QUEX S device, biofeedback

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GZO	Device, Galvanic Skin Response Measurement	Neurology	Class 2	882.1540	2025-07-18
OMC	Reduced- Montage Standard Electroencephalograph	Neurology	Class 2	882.1400	2025-07-18
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2025-07-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

White Dove Global Marketing, Ltd

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 3013755083. Last updated year: 2026. Please use registration number 3013755083 when referencing this establishment in official correspondence.