Isolife

FDA Filings

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

FDA Registration(s)
Registration Number3014980450
FEI Number3014980450
Nameisolife
Owner & Operatorisolife
Contact Address11th floor, 234, Sinheung-ro,
Uijeongbu-si KR-41 Gyeonggido 11651 KR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address11th floor, 234, Sinheung-ro,
Uijeongbu-si Gyeonggido, 11651 KR
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
isolife
Isoneck2018-11-09

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020090142463Pusan,South Korea -> Long Beach, CaliforniaNECK MASSAGE PILLOW35 CTN
2020051340587Pusan,South Korea -> Long Beach, CaliforniaNECK MASSAGE PILLOW120 CTN
2020050638681Pusan,South Korea -> Long Beach, CaliforniaNECK MASSAGE PILLOW110 CTN
2020020561039Pusan,South Korea -> Long Beach, CaliforniaNECK MASSAGE PILLOW50 CTN
2019122139648Pusan,South Korea -> Long Beach, CaliforniaNECK MASSAGE PILLOW36 CTN
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.