Pointnix Co L T D

FDA Filings

This page includes the latest FDA filings for Pointnix 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 Number3010476612
FEI Number3010476612
NamePOINTNIX CO., LTD.
Owner & OperatorPointNix Co., Ltd.
Contact Address302-303, 3F Act Twin Tower 1, 212-1 Kuro-Dong, Kuro-Ku
Seoul KR-11 Seoul Teugbyeolsi 0000 KR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address302-303, 3F Act Twin Tower 1, 212-1 Kuro-Dong, Kuro-Ku
Seoul Seoul Teugbyeolsi, 0000 KR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
POINTNIX CO., LTD
POINT 500 HD POINT500C HD2013-01-24

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