• 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 
 > 
 
118 records meeting your search criteria returned- Product Code: LWQ Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SORIN GROUP ITALIA S.R.L. CARBOMEDICS STANDARD PROSTHETIC HEART VA 10/09/2018
ST. JUDE MEDICAL PUERTO RICO, INC. SJM MASTERS SERIES HEART VALVE W/TEFLON 09/25/2018
MEDTRONIC HEART VALVE DIVISION OPEN PIVOT AP360 HEART VALVE 08/24/2018
MEDTRONIC, INC. OPEN PIVOT MECHANICAL HEART VALVE 08/20/2018
MEDTRONIC HEART VALVE DIVISION AORTIC AP 08/16/2018
MEDTRONIC, INC. AORTIC AP 07/18/2018
MEDTRONIC HEART VALVES DIVISION AORTIC AP 07/11/2018
ST. JUDE MEDICAL, INC. SJM REGENT 05/08/2018
SORIN GROUP ITALIA S.R.L. CARBOMEDICS OPTIFORM PROSTHETIC MITRAL H 05/07/2018
MEDTRONIC HEART VALVES DIVISION AORTIC AP 05/04/2018
-
-