Benq Medical Technology Corp

FDA Filings

This page includes the latest FDA filings for Benq Medical Technology Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

TAIWANGRE TAI SECURITY MARKET4116DUNS 656740313
FDA Registration(s)
Registration Number3003574554
FEI Number3003574554
NameEllin Lee
Owner & OperatorBenQ Medical Technology Corporation
Contact AddressNo.159, Shanying Rd., Guishan Dist.,
Taoyuan TW-TAO Taoyuan 33341 TW
Official Correspondent
  • Steven Shen
  • 886-3-2138899-5977
US Agent
  • Ellin Lee
  • 714 5594980
  • 714 5570200
  • ellin.lee@BenQ.com
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3200 Park Center Drive, Suite 150
Costa Mesa, CA 92626 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Ellin Lee [BenQ Medical Technology Corporation]
TriLite LED S600 Series; TriLite LS800 Series; TriLite LS810 Series2016-03-04
Ellin Lee [BenQ Medical Technology Corporation]
TriLite LS800-500B Series; TriLite LS800-500M Series2016-03-04
Ellin Lee [BenQ Medical Technology Corporation]
Dr.Max 5800 series; Dr.Max 7000 series; NOT-5600 series; Poseidon Q100 series; Poseidon Q200 series; TriMax 650NS series2002-04-30
Ellin Lee [BenQ Medical Technology Corporation]
Novel 330T series2002-04-30

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