Cardia Inc

FDA Filings

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

FDA Registration(s)
Registration Number3003215458
FEI Number3003215458
NameCARDIA INC.
Owner & OperatorCARDIA INC.
Contact Address2900 LONE OAK PARKWAY SUITE 130
EAGAN MN 55121 US
Official Correspondent
  • MIKE - CORCORAN
  • x-651-6914100-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2900 LONE OAK PARKWAY SUITE 130
EAGAN, MN 55121 US
Establishment TypeManufacture Device in the United States for Export Only



FDA Owner/Operator Registration




FDA Filings

Device
Company
DeviceDate
CARDIA INC.
Ultraseal Left Atrial Appendage Closure Device2020-01-24
CARDIA INC.
Ultrasept Septal Closure Devices2007-12-14

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Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2019090534881Hong Kong,Hong Kong -> Long Beach, CaliforniaINJECTION MACHINE1 CTN

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