TIANJIN DIADENT CO., LTD.

FDA Device Registration & Listing · TIANJIN CITY, CN · Registration 3004133229

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
3004133229
FEI Number
3004133229
Entity Name
TIANJIN DIADENT CO., LTD.
City/State/Country
TIANJIN CITY, CN
Establishment Address
No.1, Saida 3 road, Xiqing Economic-Technological Development Area, TIANJIN CITY --, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
TIANJIN DIADENT CO., LTD. (Owner Number: 9058105)
Owner / Operator Contact Address
JIAZHUANGZI CUN, DASI ZHEN, XIQING QU, TIANJIN CITY, CN-TJ --, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GUTTA PERCHA POINTS STERLI PAPER POINTS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EKM Gutta-Percha Dental Class 1 872.3850 2003-08-18
EKN Point, Paper, Endodontic Dental Class 1 872.3830 2003-08-18

Official Correspondent

WU ZHONG LIU

US Agent Details

Jim MacNee Business: USDeviceAgent.com Email: Jmacnee@USDeviceAgent.com Phone: (951) 8486626

Related Public Records

Same Entity

TIANJIN DIADENT CO., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004133229. Last updated year: 2026. Please use registration number 3004133229 when referencing this establishment in official correspondence.
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