Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013020540

FEI Number

3013020540

Entity Name

CHEMOMENT MATERIALS CO.,LTD

City/State/Country

Hefei Anhui, CN

Establishment Address

No.546-549, Renhe Industry Town, Shuangfeng Economic Development Zone, Hefei Anhui 230081, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Chemoment Materials Co.,ltd (Owner Number: 10086190)

Owner / Operator Contact Address

No.546-549, Renhe Industry Town, Shuangfeng Economic Development Zone, Hefei, CN-AH 230081, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dental Impression Material Impression tray Silicone Impression Material/ VPS Impression Material

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ELW	Material, Impression	Dental	Class 2	872.3660	2022-10-21
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2022-10-21
EID	Syringe, Restorative And Impression Material	Dental	Class 1	872.4565	2025-12-05

Official Correspondent

Mabel Lu

US Agent Details

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

Related Public Records

Same Entity

Chemoment Materials 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
K952614	Dentsply Intl.	JELTRATE PLUS ANTIMICROBIAL IMPR. MATERIAL	1996-08-13

Similar Registrations

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3030268763	OWL DENTAL	San Leandro, CA, US
8021038	VANNINI DENTAL INDUSTRY SRL	GRASSINA(FI) Firenze, IT
2018957	DEN-MAT HOLDINGS, LLC	Lompoc, CA, US
3005558160	MAXILL, INC.	ST. THOMAS Ontario, CA
9611385	Solventum Germany GmbH	SEEFELD Bavaria, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013020540. Last updated year: 2026. Please use registration number 3013020540 when referencing this establishment in official correspondence.