Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017417656

FEI Number

3017417656

Entity Name

FOSHAN NANHAI XIQIAO QIFENG SANITARY PRODUCTS CO., LTD

City/State/Country

Foshan City Guangdong, CN

Establishment Address

No.38, Baiye Avenue, Science & Technology Industrial Park, Xiqiao Town, Nanhai District, Foshan City Guangdong 528211, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Foshan Nanhai Xiqiao Qifeng Sanitary Products Co., Ltd (Owner Number: 10076557)

Owner / Operator Contact Address

No.38, Baiye Avenue, Science & Technology Industrial Park, Xiqiao Town, Nanhai District, Foshan City, CN-GD 528211, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

love-u herbday medium size saesom pantyliner love-u herbday large size saesom medium size love-u herbday pantyliner saesom large size love-u herbday medium size love-u herbday large size Atomy Herb Day Large love-u herbday pantyliner Atomy Herb Day Medium Atomy Herb Day Pantyliner love-u herbday large size love-u herbday pantyliner love-u herbday medium size

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	2020-07-23
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2020-07-23
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2020-07-23

Official Correspondent

No official correspondent registered.

US Agent Details

Uju Krallum Business: Onbix Corp US Email: onbixus@gmail.com Phone: (843) 5828036

Related Public Records

Same Entity

Foshan Nanhai Xiqiao Qifeng 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 3017417656. Last updated year: 2026. Please use registration number 3017417656 when referencing this establishment in official correspondence.