Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007740664

FEI Number

3007740664

Entity Name

Shenzhen Jiahong Dental Technology Co., Ltd

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

3/F Building A5, Fufa Industrial Park, No.3 Fuyuan 1st Road, Heping Community, Fuhai Street, Bao'an District,, Park, Fuhai Road Baoan, Shenzhen Guangdong 518103, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Shenzhen Jiahong Dental Technology Co., Ltd (Owner Number: 10029910)

Owner / Operator Contact Address

3/F Block A5, Fufa Industrial Park, NO.5 Fuyuan Rd, Heping Community, Fuhai Street, Bao An District, Shenzhen, CN-GD 518103, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EKO ELM EBG EJT ELL NHA EJT EJH

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EKO	Denture Preformed (Partially Prefabricated Denture)	Dental	Class 2	872.3600	2010-04-15
ELM	Denture, Plastic, Teeth	Dental	Class 2	872.3590	2009-07-14
EBG	Crown And Bridge, Temporary, Resin	Dental	Class 2	872.3770	2010-04-15
EJT	Alloy, Gold-Based Noble Metal	Dental	Class 2	872.3060	2010-04-15
ELL	Teeth, Porcelain	Dental	Class 2	872.3920	2009-07-14
NHA	Abutment, Implant, Dental, Endosseous	Dental	Class 2	872.3630	2010-04-15
EJT	Alloy, Gold-Based Noble Metal	Dental	Class 2	872.3060	2010-04-15
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2009-07-14

Official Correspondent

Josie Wang

US Agent Details

Peter Yang Business: JIAMEI CONSULTING INC. Email: info@jiameiconsulting.com Phone: (310) 2168437

Related Public Records

Same Entity

Shenzhen Jiahong Dental 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
K070591	Union Dental S.A./Unidesa.Odi	REPLICA, ORTOLUX TOP, ODIPAL, ODILUX, ODIDENT, VITACRILIC, NATURE'S BEST, DENTAL ACRYLIC TEETH	2007-05-11
K915276	Nobelpharma USA, Inc.	DENTURE PLASTIC TEETH,76 ELM	1992-02-03
K915626	Ivoclar North America, Inc.	EZ GOLD	1992-02-25
K211871	Faico Medical, LLC	FAICO Dental Implant System and CAD/CAM Abutments	2021-11-18
K810521	C.Vaupel Dental, Inc.	CO-SPAN 13.5 CASTING ALLOY	1981-03-17

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2018	Implant Direct Sybron Manufacturing, LLC	2	Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.

Similar Registrations

Registration Number	Establishment Name	Location
3015527834	Sonrisa/Easy Denture/NSI	Wilmington, NC, US
3009829591	JSB DENTAL, INC.	Chicago, IL, US
3030224946	GUANGZHOU JINGUANQIAO INDUSTRY CO., LTD	Guangzhou Guangdong, CN
3043303267	ONE DAY DENTAL PARTNER	Suncheon-si Jeonnam, KR
3008317118	BEST VALUE CERAMICS INC	Wyoming, PA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007740664. Last updated year: 2026. Please use registration number 3007740664 when referencing this establishment in official correspondence.