Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016733683

FEI Number

3016733683

Entity Name

Fujian JR Hygiene Products Company Limited

City/State/Country

QUANZHOU Fujian, CN

Establishment Address

NO10. Fulong south road. Fumaoling development zone,Nanan city, QUANZHOU Fujian 362300, CN

Establishment Type(s)

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

Owner / Operator

Fujian JR Hygiene Products Company Limited (Owner Number: 10063212)

Owner / Operator Contact Address

NO10. Fulong south road. Fumaoling development zone,Nanan city, QUANZHOU, CN-FJ 362300, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

soft tissues kitchen paper tissue paper facial tissues toilet paper rolls wet wipes menstrual cups face masks KN95 masks baby bib underpads dog diapers baby diapers panty liners menstrual pants baby pants baby pads adult pants dog pads adult diapers

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2021-10-13
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2021-10-13
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2021-10-13
IWO	Apron, Protective	Radiology	Class 1	892.6500	2021-10-13
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2021-10-13

Official Correspondent

Fuzhen Liang

US Agent Details

Creekon Yang Business: SPICA MEDTECH CORP Email: fda.agent@spicagloble.com Phone: (720) 6176666

Related Public Records

Same Entity

Fujian JR Hygiene Products Company Limited

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
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

Similar Registrations

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3038131023	UNITED TECHNOLOGY VIETNAM COMPANY LIMITED	Quang Ha Commune Quang Ninh, VN
3005360866	QEL DOMINICANA S.A.	ESPERANZA Valverde, DO
3043106338	SHENZHEN SPONGE NEW MATERIAL CO. LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016733683. Last updated year: 2026. Please use registration number 3016733683 when referencing this establishment in official correspondence.