Lameditech Co L T D

FDA Filings

This page includes the latest FDA filings for Lameditech Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014384451
FEI Number3014384451
NameAndrea Geffon
Owner & OperatorLAMEDITECH Co., Ltd.
Contact Address#1002, ACE High End Tower 6th, Beotkkot-
Seoul KR-11 Seoul Teugbyeolsi 08513 KR
Official Correspondent
  • Byungchul Park
  • 082-02-8527981-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address38 industrial way east, suite 1
Eatontown, NJ 07724 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Lameditech Co., Ltd.
HandyRay-Lite 2021-06-18
Lameditech Co., Ltd.
HandyRay-Pro 2020-07-09
Andrea Geffon [LAMEDITECH Co., Ltd.]
HandyRay2018-03-29
Lameditech Co., Ltd.
LMT-30002018-03-07

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