DONGGUAN CITY YUANKANG SILICON METAL PRODUCTS CO.,LTD

FDA Device Registration & Listing · Dongguan Guangdong, CN · Registration 3039261408

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3039261408
FEI Number
3039261408
Entity Name
DONGGUAN CITY YUANKANG SILICON METAL PRODUCTS CO.,LTD
City/State/Country
Dongguan Guangdong, CN
Establishment Address
No. 477,Liaobu Section,Shida Road,Liaobu Town,, Dongguan Guangdong 523000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dongguan City Yuankang Silicon Metal Products Co.,Ltd (Owner Number: 10095480)
Owner / Operator Contact Address
No. 477,Liaobu Section,Shida Road,Liaobu Town,, Dongguan, CN-GD 523000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PUMP, BREAST, NON-POWERED TOOTHBRUSH, MANUAL DROPPER, ENT DISPENSER, SOLID MEDICATION Ring, Teething, Non-Fluid Filled, Teether, Non-Fluid Filled DISPENSER, LIQUID MEDICATION

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HGY Pump, Breast, Non-Powered Obstetrics/Gynecology Class 1 884.5150 2026-03-17
EFW Toothbrush, Manual Dental Class 1 872.6855 2026-03-17
KCM Dropper, Ent Ear, Nose, Throat Class 1 874.5220 2026-03-17
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2026-03-17
MEF Ring, Teething, Non-Fluid Filled Dental Class 1 872.5550 2026-03-17
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2026-03-17

Official Correspondent

Johnney Liu

US Agent Details

Wilson Li Business: REPF America LLC Email: qagujdsvvt@outlook.com Phone: (719) 2013315

Related Public Records

Same Entity

Dongguan City Yuankang Silicon Metal Products 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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039261408. Last updated year: 2026. Please use registration number 3039261408 when referencing this establishment in official correspondence.
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