Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008544850

FEI Number

3008544850

Entity Name

JUNG CHEN TECHNOLOGY CO., LTD.

City/State/Country

Zhuhai Guangdong, CN

Establishment Address

1 Floor west, 2 Floor, Building 1, No. 2 Jinheng 2nd Road, Jinding Technology Industrial Park, Zhuhai Guangdong 519085, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Jung Chen Technology Co., Ltd (Owner Number: 10030552)

Owner / Operator Contact Address

1 Floor west, 2 Floor, Building 1, No. 2 Jinheng 2nd Road, Jinding Technology Industrial Park, Zhuhai, CN-GD 519085, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Disposable Prophy Angle AeroPro Cordless Prophy System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EHK	Cup, Prophylaxis	Dental	Class 1	872.6290	2009-10-16
EKX	Handpiece, Direct Drive, Ac-Powered	Dental	Class 1	872.4200	2025-09-16

Official Correspondent

Tina Li

US Agent Details

Jessica Huang Business: PREMIER DENTAL PRODUCTS COMPANY Email: JHuang@premierdentalco.com Phone: (610) 2396069

Related Public Records

Same Entity

Jung Chen 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
K241065	Dentis Co., Ltd.	ChecQ (AC100)	2025-03-21

Similar Registrations

Registration Number	Establishment Name	Location
3004753334	JIANGSU PROVINCE YANGZHOU SHUGUANG TOOTHBRUSH MANUFACTORY	YANG ZHOU Jiangsu, CN
1525838	ABRASIVE TECHNOLOGY, LLC	LEWIS CENTER, OH, US
3012312751	DENTAL BRANDS FOR LESS	Markham Ontario, CA
3006847937	Premium Plus International Limited	Hong Kong, HK
3004130302	MICERIUM S.P.A.	AVEGNO Genova, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008544850. Last updated year: 2026. Please use registration number 3008544850 when referencing this establishment in official correspondence.