BARON (CHINA) CO., LTD

FDA Device Registration & Listing · Quanzhou Fujian, CN · Registration 3010402957

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
3010402957
FEI Number
3010402957
Entity Name
BARON (CHINA) CO., LTD
City/State/Country
Quanzhou Fujian, CN
Establishment Address
Chengbei Industrial Park,Luocheng Town, Huian County, Quanzhou Fujian 362100, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Baron (China) CO., LTD (Owner Number: 10044261)
Owner / Operator Contact Address
Chengbei Industrial Park, Luocheng Town, Huian County, Quanzhou, CN-FJ 362100, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Disposable Face Mask Underpad baby napkin Adult Napkin

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-04-13
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2019-12-16
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2013-05-19

Official Correspondent

yangjing Zhuang

US Agent Details

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

Related Public Records

Same Entity

Baron (China) 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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010402957. Last updated year: 2026. Please use registration number 3010402957 when referencing this establishment in official correspondence.
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