HUIZHOU ANBOSON TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · huizhou Guangdong, CN · Registration 3017929385

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
3017929385
FEI Number
3017929385
Entity Name
HUIZHOU ANBOSON TECHNOLOGY CO., LTD.
City/State/Country
huizhou Guangdong, CN
Establishment Address
2 / F, factory building No.7, Hechang East 4th Road, Zhongkai hi tech Zone, Huizhou City, huizhou Guangdong 516001, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Huizhou ANBOSON Technology Co., Ltd. (Owner Number: 10079802)
Owner / Operator Contact Address
2 / F, factory building No.7, Hechang East 4th Road, Zhongkai hi tech Zone, Huizhou City, huizhou, CN-GD 516001, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Latex patient examination glove Polymer patient examination glove Disposable Examination Gloves Patient examination glove

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 2022-01-14
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2023-06-06
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2022-08-16
FMC Patient Examination Glove General Hospital Class 1 880.6250 2022-01-14

Official Correspondent

Morning Wu

US Agent Details

Yueting Zhu Email: Huanwei001@outlook.com Phone: (424) 3769142

Related Public Records

Same Entity

Huizhou ANBOSON 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
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 3017929385. Last updated year: 2026. Please use registration number 3017929385 when referencing this establishment in official correspondence.
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