Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019909974

FEI Number

3019909974

Entity Name

SHENZHEN HLD DENTAL&TECHNOLOGY CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

33 building,Lianchuang Science technology park,Longgang District, Shenzhen Guangdong 518112, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen HLD Dental&Technology Co.,Ltd (Owner Number: 10082205)

Owner / Operator Contact Address

Building 19,Lianchuang Science technology park,Longgang District, Shenzhen, CN-GD 518112, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DENTSPLY; VERTEX; Huge ARGEN; BEGO; IVOCLAR; Lucitone 199; TCS; VALPLAST; VERTEX; VITALLIUM; YAMAHACHI Heraeus; Argen Argen Heraeus; Argen IVOCLAR; UPCERA; VITA; Adite Heraeus; Argen; Vita; Ceramic; Ivoclar Shofu Heraeus; Argen; Vita; Ceramic; Ivoclar

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NSL	Dentures, Full	Unknown	Class N	N/A	2021-06-27
NSK	Dentures, Partial	Unknown	Class N	N/A	2021-06-27
EJS	Alloy, Other Noble Metal	Dental	Class 2	872.3060	2021-06-27
EJT	Alloy, Gold-Based Noble Metal	Dental	Class 2	872.3060	2021-06-27
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2021-06-27
NSP	Restoration, Porcelain	Unknown	Class N	N/A	2021-06-27
NSQ	Restoration, Base Metal	Unknown	Class N	N/A	2021-06-27
NSN	Restoration, Resin, Crown And Bridge	Unknown	Class N	N/A	2021-06-27
ELJ	Teeth, Artificial, Posterior With Metal Insert	Dental	Class 1	872.3900	2021-06-27

Official Correspondent

Tina Yuan

US Agent Details

Ben Topaz Email: cydney@goldenceramicdentallab.com Phone: (224) 7543100

Related Public Records

Same Entity

Shenzhen HLD 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
K915626	Ivoclar North America, Inc.	EZ GOLD	1992-02-25
K810521	C.Vaupel Dental, Inc.	CO-SPAN 13.5 CASTING ALLOY	1981-03-17

Similar Registrations

Registration Number	Establishment Name	Location
3030516430	DANTECH DIGITAL DENTAL SOLUTIONS PRIVATE LIMITED	Chennai Tamil Nadu, IN
3004086183	Royal Dental Lab	Shenzhen Guangdong, CN
3011714596	HK ADVANCED DENTAL DIGITAL LIMITED	Tsuen Wan, N.T, HK
3009093236	PERFECT CROWN DENTAL LAB	Maspeth, NY, US
3010594724	PREFERRED DENTAL LABORATORY, INC.	Roseland, NJ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019909974. Last updated year: 2026. Please use registration number 3019909974 when referencing this establishment in official correspondence.