• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
341 records meeting your search criteria returned- Product Code: FGE Product Problem: Premature Activation Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ZILVER 518 BILIARY SELF-EXPANDING STENT 03/17/2022
BOSTON SCIENTIFIC CORPORATION WALLSTENT RP ENDOPROSTHESIS 03/10/2022
ABBOTT VASCULAR ABSOLUTE PRO .035 SELF EXPANDING STENT S 02/24/2022
BOSTON SCIENTIFIC CORPORATION FLEXIMA BILIARY 02/01/2022
BOSTON SCIENTIFIC CORPORATION WALLSTENT RX BILIARY 01/07/2022
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG FLEXXUS ENDOSCOPIC BILIARY STENT 12/28/2021
BOSTON SCIENTIFIC CORPORATION RX BILIARY 12/14/2021
COOK IRELAND LTD EVOLUTION® BILIARY CONTROLLED-RELEASE ST 12/13/2021
ABBOTT VASCULAR ABSOLUTE PRO .035 SELF EXPANDING STENT S 12/08/2021
CORDIS CORPORATION LONG GEN / PRO 29 X 90 BIL 135 11/24/2021
-
-