Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005951296

FEI Number

3005951296

Entity Name

Jiangsu Goju Identification Technology Co., Ltd.

City/State/Country

YANCHENG CITY Jiangsu, CN

Establishment Address

2A-1,S.M.E.P,CENTURY AVE., YANDU DISTRICT, YANCHENG CITY Jiangsu 224005, CN

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Jiangsu Goju Identification Technology Co., Ltd. (Owner Number: 9090501)

Owner / Operator Contact Address

2A-1, S.M.E.P,CENTURY AVE.,YANDU, YANCHENG CITY, CN-JS 224005, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

BK070037

PMA Number

N/A

All Registered Proprietary Names

First Aid Kits Elastic Bandage Gauze bandage PBT bandage MARKING PEN Identification Wristbands Nonresorbable Gauze sponge gauze sponge GAUZE SPONGE X-RAY DETECTABLE Barcode wristband BLOOD BAND ID WRISTBAND

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2015-03-18
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2015-03-18
FZZ	Marker, Skin	General, Plastic Surgery	Class 1	878.4660	2006-08-02
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2015-03-18
GDY	Gauze/Sponge, Internal, X-Ray Detectable	General, Plastic Surgery	Class 1	878.4450	2015-03-18
KSS	Supplies, Blood-Bank	Hematology	Class 1	864.9050	2007-12-21

Official Correspondent

Shui Sheng Gong

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Jiangsu Goju Identification Technology Co., 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
K790050	Stanford Professional Products	SPONGES, STANFORD STERILE LAP	1979-01-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005951296. Last updated year: 2026. Please use registration number 3005951296 when referencing this establishment in official correspondence.