GUANGDONG CHUANTIAN SANITARY PRODUCTS CO.,LTD

FDA Device Registration & Listing · Zhongshan Guangdong, CN · Registration 3016452317

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
3016452317
FEI Number
3016452317
Entity Name
GUANGDONG CHUANTIAN SANITARY PRODUCTS CO.,LTD
City/State/Country
Zhongshan Guangdong, CN
Establishment Address
Building 2, No.46, Guangfeng Road, Torch Development Zone, Zhongshan Guangdong 528437, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Guangdong Chuantian Sanitary Products Co.,Ltd (Owner Number: 10062289)
Owner / Operator Contact Address
Building 2, No.46, Guangfeng Road, Torch Development Zone, Zhongshan, CN-GD 528437, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bladder control pad Pantyliner Sanitary Napkins Postpartum Pad

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2020-01-09
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2020-01-09

Official Correspondent

Wei Ge

US Agent Details

PEIEN LI Email: peli@kawada.com.cn Phone: (510) 6937016

Related Public Records

Same Entity

Guangdong Chuantian 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016452317. Last updated year: 2026. Please use registration number 3016452317 when referencing this establishment in official correspondence.
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