FOSHAN ZHONGROU CONSUME PRODUCTS CO., LTD

FDA Device Registration & Listing · FOSHAN Guangdong, CN · Registration 3016936908

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
3016936908
FEI Number
3016936908
Entity Name
FOSHAN ZHONGROU CONSUME PRODUCTS CO., LTD
City/State/Country
FOSHAN Guangdong, CN
Establishment Address
NO. 51, ZHANGWANG ROAD, HECHENG STREET, GAOMING DISTRICT,, FOSHAN Guangdong 528500, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
FOSHAN ZHONGROU CONSUME PRODUCTS CO., LTD (Owner Number: 10088919)
Owner / Operator Contact Address
NO. 51, ZHANGWANG ROAD, HECHENG STREET, GAOMING DISTRICT,, FOSHAN, CN-GD 528500, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

uNeat Regular 6 Pack uNeat 2X Long 6 Pack uNeat Disposable Period Underwear L/XL uNeat Mini with Wings 6 Pack uNeat Long uNeat Regular uNeat Extra Long 6 Pack uNeat 2X Long uNeat Disposable Period Underwear S/M uNeat Disposable Period Underwear XS uNeat Mini with Wings uNeat Extra Long uNeat Long 6 Pack Sanitary pads(unscented) Disposable Adult Diapers Disposable Baby Diapers

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 2023-10-20
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2023-12-12

Official Correspondent

No official correspondent registered.

US Agent Details

Ada Grant Email: alg.llc@outlook.com Phone: (425) 2605321

Related Public Records

Same Entity

FOSHAN ZHONGROU CONSUME 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 3016936908. Last updated year: 2026. Please use registration number 3016936908 when referencing this establishment in official correspondence.
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