Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004649039

FEI Number

3004649039

Entity Name

YANGZHOU HAODI ARTICLES OF EVERYDAY USE CO., LTD.

City/State/Country

YANGZHOU Jiangsu, CN

Establishment Address

53#,SITONG ROAD, YANGZHOU Jiangsu 225000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

YANGZHOU HAODI ARTICLES OF EVERYDAY USE CO., LTD. (Owner Number: 10050126)

Owner / Operator Contact Address

53#,SITONG ROAD, YANGZHOU, CN-JS 225000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Floss Pick Mask LICE COMB Toothbrush

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JES	Floss, Dental	Dental	Class 1	872.6390	2020-07-22
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	2020-04-03
LJL	Detectors And Removers, Lice, (Including Combs)	General Hospital	Class 1	880.5960	2024-01-02
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2015-10-15

Official Correspondent

Kun Wang

US Agent Details

James H. Liao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

YANGZHOU HAODI ARTICLES OF EVERYDAY USE 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
K882164	Arthur Blank & Co., Inc.	FLOSS CARD	1988-06-10
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11

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3014045831	DENTAL LACE INC.	Pittsfield, ME, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004649039. Last updated year: 2026. Please use registration number 3004649039 when referencing this establishment in official correspondence.