• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
371 records meeting your search criteria returned- Product Code: MIH Product Problem: Unintended Movement Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENDOLOGIX AFX2 04/07/2021
ENDOLOGIX AFX 04/07/2021
BOLTON MEDICAL, INC. TREO ABDOMINAL STENT-GRAFT SYSTEM 03/05/2021
W. L. GORE & ASSOCIATES, INC. GORE EXCLUDER AAA ENDOPROSTHESIS 02/22/2021
W. L. GORE & ASSOCIATES, INC. CONFORMABLE GORE TAGTHORACIC ENDOPROSTHE 02/11/2021
ENDOLOGIX AFX 12/29/2020
ENDOLOGIX AFX 12/16/2020
WILLIAM COOK EUROPE ZENITH ALPHA THORACIC ENDOVASCULAR GRAFT 12/15/2020
W. L. GORE & ASSOCIATES, INC. GORE EXCLUDER ILIAC BRANCH ENDOPROSTHESI 12/11/2020
W. L. GORE & ASSOCIATES, INC. GORE EXCLUDER AAA ENDOPROSTHESIS 12/11/2020
-
-