Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006540412

FEI Number

3006540412

Entity Name

SHANGHAI FOLIAGE INDUSTRY CO., LTD.

City/State/Country

SHANGHAI, CN

Establishment Address

2288 BAISHI RD,BAIHE TOWN, QINGPU DISTRICT, SHANGHAI 201711, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

SHANGHAI FOLIAGE INDUSTRY CO.,LTD (Owner Number: 9099120)

Owner / Operator Contact Address

2288 BAISHI ROAD,BAIHE TOWN,, QINGPU DISTRICT, SHANGHAI, CN-NOTA 201711, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PANTY LINER SANITARY NAPKIN SANITARY PADS Disposable Breast Pads Disposable Mask Pad Panty Liner SANITARY PADS

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	2007-03-16
NTX	Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68)	General Hospital	Class 1	880.5630	2019-05-08
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2007-03-16
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2012-01-29

Official Correspondent

Felix Shi

US Agent Details

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

Related Public Records

Same Entity

SHANGHAI FOLIAGE INDUSTRY 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 3006540412. Last updated year: 2026. Please use registration number 3006540412 when referencing this establishment in official correspondence.