Kyk Co L T D

FDA Filings

This page includes the latest FDA filings for Kyk 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 Number3005720077
FEI Number3005720077
NameKYK CO.,LTD
Owner & OperatorKYK Co.,Ltd
Contact Address(406,407) 555, Dunchon-daero, Jungwon-gu
Seongnam-si KR-41 Gyeonggido 13215 KR
US Agent
Importing Logistics Registration
ImporterLA KYK Alkaline Ionizer(Hyun Noh)
Address3193W. Olympic Blvd.
Los Angeles, CA 90006 UNITED STATES
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address(406,407) 555, Dunchon-daero, Jungwon-gu
Seongnam-si Gyeonggido, 13215 KR
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
KYK CO.,LTD
HYM3+2006-05-08
KYK CO.,LTD
HYDROGEN TOX12006-05-08
KYK CO.,LTD
HIGEN4+2006-05-08
KYK CO.,LTD
HIGEN32006-05-08
KYK CO.,LTD
HIGEN2+2006-05-08
KYK CO.,LTD
HIGEN1+2006-05-08

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2019122776086Pusan,South Korea -> Los Angeles, CaliforniaHYDROGEN WATER GENERATOR61 CTN
2019011575380Pusan,South Korea -> Los Angeles, CaliforniaALKALINE WATER IONIZER53 CTN
2018033124406Pusan,South Korea -> Los Angeles, CaliforniaALKALINE WATER LONIZER 8543.70 POLYESTER KNIT TED FABRIC 6004.1043 PKG
2018030338313Pusan,South Korea -> Honolulu, HawaiiALKALINE WATER IONIZER31 PKG
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