Crospon L T D

FDA Filings

This page includes the latest FDA filings for Crospon 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 Number3006897778
FEI Number3006897778
NameCROSPON LTD.
Owner & OperatorCrospon Ltd.
Contact AddressGalway Business Park Dangan
Galway IE-G Galway 00000 IE
US Agent
  • Tim Thomas
  • 770 6620870 1108
  • 770 6620510
  • Timothy.N.Thomas@Medtronic.Com
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressGalway Business Park Dangan
Galway Galway, 00000 IE
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
CROSPON LIMITED
EsoFLIP 2020-04-24
CROSPON LIMITED
EndoFLIP Loaner Unit 2019-11-08
CROSPON LIMITED
EndoFLIP 2019-11-08
CROSPON LIMITED
EndoFLIP 2019-11-08
CROSPON LIMITED
EndoFLIP 2019-11-08
CROSPON LIMITED
EndoFLIP 2019-11-08
CROSPON LIMITED
EndoFLIP 2019-11-08
CROSPON LTD.
Flip Topography Module2019-08-20
CROSPON LTD.
EndoFlip System2019-08-20
CROSPON LTD.
EndoFlip Catheter2019-08-20
CROSPON LTD.
EsoFlip Catheter2019-08-20
CROSPON LTD.
ES-3102019-08-20
Crospon Ltd
EndoFLIP System2019-02-15
CROSPON LIMITED
EsoFLIP 2018-07-06
CROSPON LIMITED
EsoFLIP 2018-07-06
Crospon Ltd.
EsoFLIP® ES-310 Balloon Catheter2017-11-22
Crospon Ltd.
EndoFLIP® System With FLIP Topography Module2017-04-17
CROSPON LTD.
EndoFLIP2016-05-01
CROSPON LTD.
EsoFLIP2014-12-19
CROSPON LTD.
ES-3202014-12-19
CROSPON, LTD.
ESOFLIP ES2014-09-25
CROSPON LTD.
EsoFLIP2014-01-06
CROSPON LTD.
ES-3302014-01-06
CROSPON LTD.
EsoFLIP2014-01-06
CROSPON LTD.
ES-3302014-01-06
CROSPON, LTD.
ESOFLIP BALLOON DILATION CATHETER2013-10-07
CROSPON, LTD.
ENDOFLIP CATHETER2013-07-17
CROSPON, LTD.
BAROSTAT SOFTWARE OPTION2012-08-27
CROSPON, LTD.
ENDOFLIP ECD2011-10-06
CROSPON, LTD.
ENDOFLIP GASTRIC TUBE2011-07-22
CROSPON, LTD.
ENDO FLIP2010-12-16
CROSPON, LTD.
ENDOFLIP2009-12-15

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