Fistula Solution Corp

FDA Filings

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

FDA Registration(s)
Registration Number3010521015
FEI Number3010521015
NameFISTULA SOLUTION CORPORATION
Owner & OperatorFistula Solution Corporation
Contact Address10604 230th Street North
Scandia MN 55073 US
Official Correspondent
  • Andrew T Obst
  • 1-844-5284479-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address10604 230TH ST N
Scandia, MN 55073 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
Fistula Solution Corporation
 Isolation Device Mixed pack 008600130003942023-12-08
Fistula Solution Corporation
 Isolator Strip 008600130003182022-08-29
Fistula Solution Corporation
 Fistula Funnel 008600130003252022-08-29
Fistula Solution Corporation
 Wound Crown 008600130003012022-08-29
FISTULA SOLUTION CORPORATION
Wound Crown2013-10-23
FISTULA SOLUTION CORPORATION
Isolator Strip2013-10-23
FISTULA SOLUTION CORPORATION
Fistula Funnel2013-10-23

Related Finance Registrations
NCAGE Code7M5P2FISTULA SOLUTION CORPORATION
CAGE Code7M5P2FISTULA SOLUTION CORPORATION
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