SHANGHAI JINXIANG LATEX PRODUCTS CO., LTD.

FDA Device Registration & Listing · SHANGHAI, CN · Registration 8043142

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
8043142
FEI Number
3332
Entity Name
SHANGHAI JINXIANG LATEX PRODUCTS CO., LTD.
City/State/Country
SHANGHAI, CN
Establishment Address
No. 36,Leizhou Road, Xinghuo Development, Fengxian District, SHANGHAI 201419, CN
Establishment Type(s)
Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SHANGHAI JINXIANG LATEX PRODUCTS CO., LTD. (Owner Number: 8043142)
Owner / Operator Contact Address
No. 36,Leizhou Road, Xinghuo Development, Fengxian District, SHANGHAI, CN-SH 201419, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Patient Examination Gloves (Latex) Profect Examination Gloves

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2012-12-26
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2012-12-26

Official Correspondent

Lijun Shan

US Agent Details

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

Related Public Records

Same Entity

SHANGHAI JINXIANG LATEX PRODUCTS 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
K894452 Kerala Rubber & Reclaims, Ltd. KRR GLOVE, PATIENT EXAMINATION GLOVES 1989-08-09
K891323 Li Wah-Hong Kong, Inc. LI WAH LATEX EXAMINATION GLOVES 1989-08-31
K891418 C & K Mfg. & Sales Co. LATEX EXAMINATION GLOVES, STYLE 510 LX 1989-06-22
K994255 Pt. Maja Agung Latexindo LATEX EXAMINATION GLOVES-PRE-POWDERED-STERILE 2000-02-07
K892946 Yeou-Fwu Rubber Industrial Co., Ltd. STERILE PATIENT EXAMINATION GLOVES 1989-08-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043142. Last updated year: 2026. Please use registration number 8043142 when referencing this establishment in official correspondence.
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