QUANZHOU HUIFENG SANITARY ARTICLES CO.,LTD

FDA Device Registration & Listing · QUANZHOU Fujian, CN · Registration 3013511504

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
3013511504
FEI Number
3013511504
Entity Name
QUANZHOU HUIFENG SANITARY ARTICLES CO.,LTD
City/State/Country
QUANZHOU Fujian, CN
Establishment Address
NO.2 JINSHI ROAD, SHUANGYANG STREET, LUOJIANG, QUANZHOU Fujian 362000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
QUANZHOU HUIFENG SANITARY ARTICLES CO.,LTD (Owner Number: 10053255)
Owner / Operator Contact Address
NO.2 JINSHI ROAD, SHUANGYANG STREET, LUOJIANG, QUANZHOU, CN-FJ 362000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KHA Mask, Scavenging Anesthesiology Class 1 868.5590 2020-03-05
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2020-04-17
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 2020-04-17
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2016-11-15

Official Correspondent

Xinzhan Lai

US Agent Details

Kai Li Email: likai323@hotmail.com Phone: (501) 7778490

Related Public Records

Same Entity

QUANZHOU HUIFENG SANITARY ARTICLES 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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

Similar Registrations

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3017654286 GUANGDONG BINGBING HEALTH CARE PRODUCTS LTD. Jiangmen Guangdong, CN
3011424870 XIANTAO KIMBERLY PROTECTIVE PRODUCTS CO., LTD Xiantao Hubei, CN
3008808082 PLANET(SHANGHAI) INTERNATIONAL CO.,LTD shanghai, CN
3012436532 HEFEI ANAN TRADE DEVELOPMENT CO. LTD. Hefei Anhui, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013511504. Last updated year: 2026. Please use registration number 3013511504 when referencing this establishment in official correspondence.
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