Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013518061

FEI Number

3013518061

Entity Name

XIAMEN NEWCLEARS DAILY PRODUCTS CO.,LTD.

City/State/Country

Xiamen Fujian, CN

Establishment Address

Unit 101, No.600 Guankou South Road, Jimei District, Xiamen Fujian 361000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Xiamen Newclears Daily Products Co.,Ltd. (Owner Number: 10054695)

Owner / Operator Contact Address

Unit 101, No.600 Guankou South Road, Jimei District, Xiamen, CN-FJ 361000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pet pad Baby diaper,baby pull up,adult diaper,adult pull up Underpad Sanitary napkin Wet wipe Disposable Face mask,Face mask,Isolation mask, Mask

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2017-04-16
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2017-04-16
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2017-04-16
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2017-04-16
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2020-03-23

Official Correspondent

Lin Lin

US Agent Details

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

Related Public Records

Same Entity

Xiamen Newclears Daily 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 3013518061. Last updated year: 2026. Please use registration number 3013518061 when referencing this establishment in official correspondence.