Yangzhou Yichuan Plastic Technology Co., Ltd.

FDA Device Registration & Listing · Yangzhou City Jiangsu, CN · Registration 3013123677

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
3013123677
FEI Number
3013123677
Entity Name
Yangzhou Yichuan Plastic Technology Co., Ltd.
City/State/Country
Yangzhou City Jiangsu, CN
Establishment Address
No.1, Kechuang Garden, Gaoyou town, No.2 Dongyuan road, Gaoyou City, Yangzhou City Jiangsu 225600, 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 Yichuan Plastic Technology Co., Ltd. (Owner Number: 10050718)
Owner / Operator Contact Address
No.1, Kechuang Garden, Gaoyou town, No.2 Dongyuan road, Gaoyou City, Yangzhou City, CN-JS 225600, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Periodontic Hoe Dental floss Adult Toothbrush, Child Toothbrush, Travel Toothbrush, Tongue brush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EMQ Hoe, Periodontic Dental Class 1 872.4565 2015-12-18
JES Floss, Dental Dental Class 1 872.6390 2015-12-18
EFW Toothbrush, Manual Dental Class 1 872.6855 2015-12-18
LCN Scraper, Tongue Dental Class 1 872.6855 2015-12-18

Official Correspondent

Jianzheng Mao

US Agent Details

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

Related Public Records

Same Entity

Yangzhou Yichuan Plastic Technology 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013123677. Last updated year: 2026. Please use registration number 3013123677 when referencing this establishment in official correspondence.
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