Urocure L L C

FDA Filings

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

FDA Registration(s)
Registration Number3013859837
FEI Number3013859837
NameUROCURE, LLC
Owner & OperatorUroCure, LLC
Contact Address701 North 3rd Street Suite 110
Minneapolis MN 55401 US
Official Correspondent
  • Sara Petrie
  • x-612-3969849-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address701 North 3rd Street Suite 110
Minneapolis, MN 55401 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
UroCure LLC
ArcSP Suprapubic Sling System2022-09-21
UroCure LLC
ArcTO Transobturator Sling System2022-09-15
UROCURE LLC
ArcTV™ Transvaginal Sling System A-TV-10012019-08-21
UROCURE, LLC
ArcTV Transvaginal Sling System2019-07-31
UroCure LLC
ArcTV Transvaginal Sling System2019-02-07

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