Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022582361

FEI Number

3022582361

Entity Name

MEIXIN (ANHUI) SANITARY PRODUCTS CO.,LTD

City/State/Country

Chuzhou Anhui, CN

Establishment Address

No.6,Heying Road, Chuzhou Anhui 239000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Meixin (Anhui) Sanitary Products Co.,LTD (Owner Number: 10084744)

Owner / Operator Contact Address

No.6,Heying Road, Chuzhou, CN-AH 239000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tampom Diapers

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2022-03-28
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2022-03-28

Official Correspondent

JinLong Huang

US Agent Details

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

Related Public Records

Same Entity

Meixin (Anhui) Sanitary 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
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28

Similar Registrations

Registration Number	Establishment Name	Location
3029303082	ROUTINE LLC	Alpharetta, GA, US
3017021601	COAM, Inc.	Coppell, TX, US
3016654531	SEKHANI INDUSTRIES PVT LTD	Ahmedabad Gujarat, IN
9615625	KIMBERLY-CLARK PERSONAL HYGIENIC PRODUCTS CO.,LTD.BEIJING	DEVELOPMENT ZONE, BEIJING, CN
3017366514	FIBRIL TEX PVT LTD.	Amritsar Punjab, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022582361. Last updated year: 2026. Please use registration number 3022582361 when referencing this establishment in official correspondence.