Ellin Lee

FDA Filings

This page includes the latest FDA filings for Ellin Lee. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3003574554
• FEI Number: 3003574554
• Name: Ellin Lee
• Owner & Operator: BenQ Medical Technology Corporation
• Contact Address: No.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 Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 3200 Park Center Drive, Suite 150 ; Costa Mesa, CA 92626 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
FSY Ellin Lee [BenQ Medical Technology Corporation]	TriLite LED S600 Series; TriLite LS800 Series; TriLite LS810 Series	2016-03-04
FSS Ellin Lee [BenQ Medical Technology Corporation]	TriLite LS800-500B Series; TriLite LS800-500M Series	2016-03-04
GDC 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 series	2002-04-30
FWX Ellin Lee [BenQ Medical Technology Corporation]	Novel 330T series	2002-04-30