Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014657561

FEI Number

3014657561

Entity Name

Dongguan Q & S Electronic Manufacturing Company Limited

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Yin Shan District, Fu Gang Village, Xiang Mang West Road, Qing Xi Town, Dongguan Guangdong 523660, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

EWIG Industries International Co. Limited (Owner Number: 10083533)

Owner / Operator Contact Address

Avenida Da Praia Grande No. 619, EDF.Comercial Si Toi L6, Macau, CN-MO 999078, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Exerciser, measuring PERINEOMETER CENTRIFUGES (MICRO, ULTRA, REFRIGERATED) FOR CLINICAL USE AID, TRANSFER Vibrator for therapeutic use, genital PERINEOMETER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISD	Exerciser, Measuring	Physical Medicine	Class 2	890.5360	2021-11-29
HIR	Perineometer	Obstetrics/Gynecology	Class 2	884.1425	2024-04-11
JQC	Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use	Clinical Chemistry	Class 1	862.2050	2022-05-29
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2023-08-08
KXQ	Vibrator For Therapeutic Use, Genital	Obstetrics/Gynecology	Class 2	884.5960	2021-12-20
HIR	Perineometer	Obstetrics/Gynecology	Class 2	884.1425	2024-04-14

Official Correspondent

Alex Chong

US Agent Details

Heng Zhang Business: YOUKE E-COMMERCE INC Email: youkecommerce@hotmail.com Phone: (720) 7609666

Related Public Records

Same Entity

EWIG Industries International Co. Limited

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014657561. Last updated year: 2026. Please use registration number 3014657561 when referencing this establishment in official correspondence.