ASCEND EXCELLENCE DAILY PRODUCTS JIANGSU CO., LTD

FDA Device Registration & Listing · Yangzhou Jiangsu, CN · Registration 3012590871

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
3012590871
FEI Number
3012590871
Entity Name
ASCEND EXCELLENCE DAILY PRODUCTS JIANGSU CO., LTD
City/State/Country
Yangzhou Jiangsu, CN
Establishment Address
Room 1010, Block 1, Fengchuang Mansion, West of Runyang Rd & South of Jiangyang West Rd, Hanjiang District, Yangzhou Jiangsu 225009, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Ascend Excellence Daily Products Jiangsu Co., Ltd (Owner Number: 10055626)
Owner / Operator Contact Address
Room 1010, Block 1, Fengchuang Mansion, West of Runyang Rd & South of Jiangyang West Rd, Hanjiang District, Yangzhou, CN-JS 225009, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Toothbrush Ascend Ascend Dental Floss, Floss Pick Ascend Scraper, Tongue Cleaner Ascend Dental Guard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 2017-08-25
JES Floss, Dental Dental Class 1 872.6390 2017-08-25
LCN Scraper, Tongue Dental Class 1 872.6855 2019-12-05
EEJ Guard, Disk Dental Class 1 872.6010 2021-01-07

Official Correspondent

Tao Xu

US Agent Details

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

Related Public Records

Same Entity

Ascend Excellence Daily Products Jiangsu 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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012590871. Last updated year: 2026. Please use registration number 3012590871 when referencing this establishment in official correspondence.
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