Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017189554

FEI Number

3017189554

Entity Name

GUANGDONG LAUNCA MEDICAL DEVICE TECHNOLOGY CO., LTD.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Room 901-908 and 914-916, Building 5, No.1 Yanfa Road, Songshan Lake Park, Dongguan Guangdong 523808, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Guangdong Launca Medical Device Technology Co., Ltd. (Owner Number: 10074639)

Owner / Operator Contact Address

Room 901-908 and 914-916, Building 5, No.1 Yanfa Road, Songshan Lake Park, Dongguan, CN-GD 523808, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Intraoral Scanner DL-202,DL-206,DL-206P,DL-300,DL-300P,DL-300 Wireless,Dualscan,Breezyscan

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOF	System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	Dental	Class 2	872.3661	2020-06-02

Official Correspondent

Ziyin Ye

US Agent Details

Barry Jiang Business: Grace 99, Inc. Email: citdolphin@gmail.com Phone: (626) 7251959

Related Public Records

Same Entity

Guangdong Launca Medical Device Technology 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 3017189554. Last updated year: 2026. Please use registration number 3017189554 when referencing this establishment in official correspondence.