Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006542627

FEI Number

3006542627

Entity Name

Guangdong Kawada Sanitary Products Co.,Ltd. Southern District Branch Company.

City/State/Country

GUANG DONG Guangdong, CN

Establishment Address

No. 38th, ChengNanWu Rd., Southern District,, TOWN ZHONG SHAN CITY, GUANG DONG Guangdong 528455, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

FUBURG INDUSTRIAL CO., LTD. (Owner Number: 9102559)

Owner / Operator Contact Address

No.14, Lane 205, Section.2, Nanshan Road, Luzhu district, Taoyuan, TW-TAO 33852, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Maxi Maxi Maxi Maxi Maxi

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	2007-06-08
CEN	Dye-Indicator, Ph (Urinary, Non-Quantitative)	Clinical Chemistry	Class 1	862.1550	2012-03-21
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2007-06-08
HHL	Pad, Menstrual, Scented, Scented-Deodorized	Obstetrics/Gynecology	Class 2	884.5425	2022-08-21
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2008-11-20

Official Correspondent

Fen huang

US Agent Details

Jian Wang Business: Yanjan USA LLC Email: Jianw@yanjan-usa.com Phone: (704) 8854758

Related Public Records

Same Entity

FUBURG INDUSTRIAL 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 3006542627. Last updated year: 2026. Please use registration number 3006542627 when referencing this establishment in official correspondence.