FUJIAN PUTIAN LICHENG PAPER INDUSTRY CO., LTD

FDA Device Registration & Listing · Putian Fujian, CN · Registration 3011497535

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
3011497535
FEI Number
3011497535
Entity Name
FUJIAN PUTIAN LICHENG PAPER INDUSTRY CO., LTD
City/State/Country
Putian Fujian, CN
Establishment Address
Jiaoxi Village, Huating, Chengxiang District,, Putian Fujian 351139, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Fujian Putian Licheng Paper Industry Co., Ltd (Owner Number: 10047946)
Owner / Operator Contact Address
Jiaoxi Village, Huating, Chengxiang District,, Putian, CN-FJ 351139, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Wipe Underpad,Pet Pad spill prevention breast pad Dimples by K2 Health Products, poly ethylene film, Incontinence pads Adult Diaper, Baby Diaper, Pet Diaper, Pull-up Diaper, Adult pants diaper; Baby pants diaper; Lady pants diaper,

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 2017-11-18
NTX Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) General Hospital Class 1 880.5630 2014-11-19
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2014-11-19

Official Correspondent

Yuanjian Lin

US Agent Details

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

Related Public Records

Same Entity

Fujian Putian Licheng Paper Industry Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011497535. Last updated year: 2026. Please use registration number 3011497535 when referencing this establishment in official correspondence.
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