Lorte Technologies Inc

FDA Filings

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

FDA Registration(s)
Registration Number3006305468
FEI Number3006305468
NameLORTE TECHNOLOGIES INC
Owner & OperatorLorte Technologies Inc
Contact Address1616 barclay blvd
Buffalo Grove IL 60089 US
Official Correspondent
  • George Sun
  • 1-847-2340754-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address1616 Barclay Blvd
Buffalo Grove, IL 60089 US



FDA Filings

Device
Company
DeviceDate
LORTE TECHNOLOGIES, INC
FaceLake 2020-12-17
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-07-06
LORTE TECHNOLOGIES, INC
FaceLake 2018-03-29
LORTE TECHNOLOGIES, INC
FaceLake 2018-03-29
LORTE TECHNOLOGIES, INC
FaceLake 2018-03-29
LORTE TECHNOLOGIES, INC
FaceLake 2018-03-29

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2018031015654Luda,China (Mainland) -> Long Beach, CaliforniaPULSE OXIMETER POCKET FETAL DOPPLER PORTABLE .351 CTN
2018030928894Luda,China (Mainland) -> Long Beach, CaliforniaPULSE OXIMETER POCKET FETAL DOPPLER PORTABLE .351 CTN

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