L E West L T D

FDA Filings

This page includes the latest FDA filings for L E West 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 Number3003912713
FEI Number3003912713
NameJoe Imburgio
Owner & OperatorL.E. WEST LTD
Contact AddressUnit 18, The IO Centre 59-71 River Road
BARKING, LONDON GB-NOTA IG11 0DR GB
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4360 Oakes Road Suite 613
Davie, FL 33314 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Joe Imburgio [L.E. WEST LTD]
Life Raft First Aid Kit2008-04-01

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2019112618749Port Bustamante,Jamaica -> Houston, TexasEMPTY OXYGEN BOTTLES6 BOT
2019090759857Alert Bay, BC,Canada -> Seattle, WashingtonPICCOLO ANALIZER MADE IN UNITED STATES1 BOX
2019083162843Alert Bay, BC,Canada -> Seattle, WashingtonMEDICAL EQUIPMENT MADE IN UNITED STATES1 BOX
2019030455438Marsh Harbour,Bahamas -> Port Everglades, FloridaEXPIRED METALYSE 1 VIAL PER BOX MADE IN GREAT BRITAIN2 BOX
2019011250438Kralendijk,Netherland Antilles -> Port Everglades, Florida2 TENECTEPLASE 10000 UNITS VIAL MADE IN GERMANY1 BOX
2018101625207High Seas (Outside U.S. Territorial Waters),United States Off-Shore Tanker Transshipment Points -> Boston, MassachusettsTENECTEPLASE INJECTION EXPIRED VIAL EXCHANGE1 BOX
2018043056877London,United Kingdom -> Port Everglades, FloridaNOT DANGEROUS SOLUTIONS (DRIP BAGS) IN TRANSIT TO CCL MULTIPLE VESSELS12 PCS
2018020970830San Lucas,Mexico -> San Diego, CaliforniaTENECTPLASE MADE IN GERMANY1 BOX

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