Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 3 
 > 
 
30 records meeting your search criteria returned- Product Code: FGE Patient Problem: Reocclusion Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION WALLSTENT ENDOPROSTHESIS WITH UNISTEP PL 12/16/2020
BOSTON SCIENTIFIC CORPORATION EXPRESS VASCULAR SD 11/18/2020
BOSTON SCIENTIFIC CORPORATION WALLSTENT ENDOPROSTHESIS WITH UNISTEP PL 10/05/2020
BOSTON SCIENTIFIC CORPORATION EPIC BILIARY 07/06/2020
BOSTON SCIENTIFIC CORPORATION EXPRESS LD VASCULAR 04/09/2020
COOK IRELAND LTD ZILVER 635 SELF-EXPANDING BILIARY STENT 11/22/2019
CORDIS CASHEL UNKNOWN SMARTFLEX STENT 11/07/2019
CORDIS CASHEL UNKNOWN SMART FLEX 11/07/2019
CORDIS CASHEL UNKNOWN SMART FLEX 11/07/2019
CORDIS CASHEL UNKNOWN SMARTFLEX STENT 11/07/2019
-
-