Medivance Instruments L T D

FDA Filings

This page includes the latest FDA filings for Medivance Instruments 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 Number3003982003
FEI Number3003982003
NameMEDIVANCE INSTRUMENTS LTD.
Owner & OperatorMEDIVANCE INSTRUMENTS LTD.
Contact AddressBARRETT'S GREEN ROAD --
HARLESDEN, LONDON GB-NOTA NW10 7AP GB
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressBARRETTS GREEN ROAD
HARLESDEN, LONDON London, City of, NW10 7AP GB
Establishment TypeManufacture Medical Device



Registration Number3003697084
FEI Number3003697084
NameVELOPEX INTERNATIONAL, INC.
Owner & OperatorMEDIVANCE INSTRUMENTS LTD.
Contact AddressBARRETT'S GREEN ROAD --
HARLESDEN, LONDON GB-NOTA NW10 7AP GB
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address105 EAST 17TH ST.
Saint Cloud, FL 34769 US



FDA Filings

Device
Company
DeviceDate
MEDIVANCE INSTRUMENTS LIMITED
ExtraXtender Film Processor I/MAC1017F2022-08-15
MEDIVANCE INSTRUMENTS LIMITED
IntraX Film Processor I/MAC2016F2022-08-15
MEDIVANCE INSTRUMENTS LIMITED
Velopex AquaCut Fluid Abrasion Unit I/MAC8502F /I/MAC8503F /I/MAC8508F2022-08-15
MEDIVANCE INSTRUMENTS LTD.
Extra/Xtender & Sprint Processor2012-10-12
MEDIVANCE INSTRUMENTS LTD.
IntraX FilmProcessor2010-04-14
MEDIVANCE INSTRUMENTS LTD.
Aquacut Quattro2009-10-19
MEDIVANCE INSTRUMENTS LTD.
AquaCare, AquaCare Twin2009-10-19

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