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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
450 records meeting your search criteria returned- Product Code: MIH Product Problem: Use of Device Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENDOLOGIX AFX 05/07/2021
ENDOLOGIX AFX2 04/29/2021
ENDOLOGIX SANTA ROSA OVATION IX 04/26/2021
MEDTRONIC IRELAND ENDURANT II AUI STENT GRAFT 04/13/2021
W. L. GORE & ASSOCIATES, INC. GORE EXCLUDERAAA ENDOPROSTHESIS 03/25/2021
ENDOLOGIX AFX 03/24/2021
W. L. GORE & ASSOCIATES, INC. CONFORMABLE GORE TAGTHORACIC ENDOPROSTHE 02/11/2021
W. L. GORE & ASSOCIATES, INC. GORE EXCLUDER AAA ENDOPROSTHESIS 02/11/2021
ENDOLOGIX AFX 02/08/2021
ENDOLOGIX SANTA ROSA OVATION ALTO 02/03/2021
-
-