KAWADA (ZHEJIANG) SANITARY PRODUCTS CO., LTD

FDA Device Registration & Listing · HUZHOU Zhejiang, CN · Registration 3007696018

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
3007696018
FEI Number
3007696018
Entity Name
KAWADA (ZHEJIANG) SANITARY PRODUCTS CO., LTD
City/State/Country
HUZHOU Zhejiang, CN
Establishment Address
NO.188, ZHENXI SOUTH ROAD, YUYUE TOWN, DEQING COUNTY, HUZHOU Zhejiang 313213, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Kawada (Zhejiang) Sanitary Products Co., LTD (Owner Number: 10086051)
Owner / Operator Contact Address
NO.188, ZHENXI SOUTH ROAD, YUYUE TOWN, DEQING COUNTY, HUZHOU, CN-ZJ 313213, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Breast pads Sanitary napkins, Panty liner, Menstrual pants, Meternal towel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NTX Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) General Hospital Class 1 880.5630 2022-10-12
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2022-10-12

Official Correspondent

YIRUN ZHOU

US Agent Details

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

Related Public Records

Same Entity

Kawada (Zhejiang) 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 3007696018. Last updated year: 2026. Please use registration number 3007696018 when referencing this establishment in official correspondence.
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