FUJIAN LIAO PAPER CO., LTD

FDA Device Registration & Listing · Quanzhou Fujian, CN · Registration 3016764687

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
3016764687
FEI Number
3016764687
Entity Name
FUJIAN LIAO PAPER CO., LTD
City/State/Country
Quanzhou Fujian, CN
Establishment Address
4TH DISTRICT, NORTHERN INDUSTRIAL PARK, LUOYANG TOWN, TAIWANESE INVESTMENT ZONE, Quanzhou Fujian 362121, CN
Establishment Type(s)
Manufacture Medical Device,Repack or Relabel Medical Device
Owner / Operator
Fujian LiAo Paper Co., Ltd (Owner Number: 10082479)
Owner / Operator Contact Address
4TH DISTRICT, NORTHERN INDUSTRIAL PARK, LUOYANG TOWN, TAIWANESE INVESTMENT ZONE, Quanzhou, CN-FJ 362121, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Wet wipes: 1 - 150 pieces tissue: 5-600 pieces menstrual pant: S, M, L, XL, XXL Sanitary pad: 150mm-450mm Baby Pant: S-XXXL Baby Diaper: NB-7XL adult pant: S-XXXL pet diaper: XXS, XS, S, M, L, XL, XXL, XXXL under pad: Length: 45 - 60 cm Width: 33 - 90 cm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2025-12-04
IDZ Cassettes, Tissue Pathology Class 1 864.3010 2025-12-04
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2025-12-04
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2021-08-02
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2025-12-04

Official Correspondent

Mini Cen

US Agent Details

BOBOIGE JACLINE Email: boboigechen@gmail.com Phone: (414) 9442888

Related Public Records

Same Entity

Fujian LiAo Paper 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 3016764687. Last updated year: 2026. Please use registration number 3016764687 when referencing this establishment in official correspondence.
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