Jiangsu Noda Sanitary Products Co., Ltd.

FDA Device Registration & Listing · Changzhou City Jiangsu, CN · Registration 3015220944

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
3015220944
FEI Number
3015220944
Entity Name
Jiangsu Noda Sanitary Products Co., Ltd.
City/State/Country
Changzhou City Jiangsu, CN
Establishment Address
No. 100, Dingjia Road, Xingchen Village Committees, Hengshanqiao Town, Economic Development Zone, Changzhou City Jiangsu 213119, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Jiangsu Noda Sanitary Products Co., Ltd. (Owner Number: 10059639)
Owner / Operator Contact Address
No. 100, Dingjia Road, Xingchen Village Committees, Hengshanqiao Town, Economic Development Zone, Changzhou City, CN-JS 213119, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pad, menstrual, unscented GARMENT, PROTECTIVE, FOR INCONTINENCE NURSING PAD, POLYURETHANE PAD WITH STARCH COPOLYMER, GLYCERIN, AND SURFACTANT (F-68)

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 2019-02-06
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2019-02-06
NTX Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) General Hospital Class 1 880.5630 2019-02-06

Official Correspondent

NING SUN

US Agent Details

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

Related Public Records

Same Entity

Jiangsu Noda 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 3015220944. Last updated year: 2026. Please use registration number 3015220944 when referencing this establishment in official correspondence.
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