Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014198412

FEI Number

3014198412

Entity Name

HUBEI KIMSOUL INDUSTRIAL CO.,LTD

City/State/Country

Xiantao Hubei, CN

Establishment Address

NO.1 Guohezhen industrial zone, Xiantao Hubei 433000, CN

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

HUBEI KIMSOUL INDUSTRIAL CO.,LTD (Owner Number: 10066643)

Owner / Operator Contact Address

NO.1 Guohezhen industrial zone, Xiantao, CN-HB 433000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Surgical Face Mask (Non-sterile);Model:2020,2030 3D face mask Coverall isolation gown Disposable face mask

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FXX	Mask, Surgical	General, Plastic Surgery	Class 2	878.4040	2021-12-20
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2022-07-19
OEA	Non-Surgical Gown	General, Plastic Surgery	Class 1	878.4040	2020-04-02
QKR	Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua	Unknown	Class N	N/A	2020-04-02

Official Correspondent

Faming zhang

US Agent Details

FANFEI LIU Email: U.S.agent@frosatechnology.com Phone: (626) 8261385

Related Public Records

Same Entity

HUBEI KIMSOUL INDUSTRIAL 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
K201622	Guangdong Kingfa Sci. & Tech.Co., Ltd.	Medical surgical mask	2020-11-24
K881618	3M Company	ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK	1988-05-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014198412. Last updated year: 2026. Please use registration number 3014198412 when referencing this establishment in official correspondence.