Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007695022

FEI Number

3007695022

Entity Name

Guangdong Winburg Technology Co.,Ltd

City/State/Country

ZHONGSHAN Guangdong, CN

Establishment Address

1F Factory building,No 1,Yihui Fifth Road,Henglan Town,Zhongshan City,Guangdong Province,China, ZHONGSHAN Guangdong 528478, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Guangdong Winburg Technology Co.,Ltd (Owner Number: 10029014)

Owner / Operator Contact Address

1F Factory building,No 1,Yihui Fifth Road,Henglan Town, ZHONGSHAN, CN-GD 528478, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BF990 BF857BT-ITO WW912F WW910 WW65Y WW721 WW711 WW706F EB824A GS05 EB503 EB530 BY80 EB523 EB522

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUH	Analyzer, Body Composition, Exempt	Cardiovascular	Class 2	870.2770	2018-08-09
FRI	Scale, Stand-On, Patient	General Hospital	Class 1	880.2700	2012-08-01
FRW	Scale, Patient	General Hospital	Class 1	880.2720	2009-03-30

Official Correspondent

Su Sheng

US Agent Details

James H. Liao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

Guangdong Winburg Technology Co.,Ltd

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 3007695022. Last updated year: 2026. Please use registration number 3007695022 when referencing this establishment in official correspondence.