Vivorte Inc

FDA Filings

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

FDA Registration(s)
Registration Number3010642815
FEI Number3010642815
NameVIVORTE, INC
Owner & OperatorVivorte, Inc.
Contact Address1044 E Chestnut St
Louisville KY 40204 US
Official Correspondent
  • Steven C Guenthner
  • 1-502-8192789-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1044 E Chestnut St
Louisville, KY 40204 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Vivorte, Inc
Wizard CaP 2021-08-06
Vivorte, Inc
Wizard CaP 2021-08-06
Vivorte, Inc
Wizard CaP 2021-08-06
Vivorte, Inc
Trabexus® 130703-052021-07-30
Vivorte, Inc
Trabexus® 130703-032021-07-30
Vivorte, Inc
Fortera 2020-05-22
Vivorte, Inc
Fortera 131133-05-S2020-05-22
Vivorte, Inc
Fortera 131133-03-S2020-05-22
Vivorte, Inc
Trabexus ® 131133-102018-03-29
Vivorte, Inc
Trabexus ® 131133-052018-03-29
Vivorte, Inc
Trabexus ® 131133-032018-03-29
VIVORTE, INC
Vivorte Trabexus2015-01-14
VIVORTE, INC
Vivorte Trabexus EB2015-01-14
VIVORTE, INC [Vivorte, Inc.]
Wizard CaP2014-08-04
VIVORTE, INC [Vivorte, Inc.]
Fortera2014-08-04
VIVORTE, INC [Vivorte, Inc.]
Trabexus2014-08-04
VIVORTE, INC [Vivorte, Inc.]
Trabexus2014-08-04
VIVORTE, INC
VIVORTE BVF2013-09-12
VIVORTE, INC
VIVORTE BVF LITE2013-08-12

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.