Daejong Meditec

FDA Filings

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

FDA Registration(s)
Registration Number3015472059
FEI Number3015472059
NameDAEJONG MEDITEC
Owner & OperatorDAEJONG MEDITEC
Contact Address809 Humanteco 57 Achasanro 17ga Seongdon
Seoul KR-11 Seoul Teugbyeolsi 04799 KR
Official Correspondent
  • Jang-Eui Hong
  • 82-22-2748077-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address809 Humanteco 57 Achasanro 17ga Seongdong gu Seoul
Seoul Seoul Teugbyeolsi, 04799 KR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
DAEJONG MEDITEC
needle holder2019-05-07

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