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

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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 
 
98 records meeting your search criteria returned- Product Code: LWR Patient Problem: Pulmonary Regurgitation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC HEART VALVES DIVISION HANCOCK 02/16/2016
MEDTRONIC HEART VALVES DIVISION MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 02/12/2016
MEDTRONIC HEART VALVES DIVISION HANCOCK 11/24/2015
MEDTRONIC HEART VALVES DIVISION HANCOCK 06/01/2015
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 11/18/2014
SORIN GROUP CANADA INC., MITROFLOW DIVIS MITROFLOW 07/28/2014
ST. JUDE MEDICAL SJM EPIC STENTED PORCINE HEART VALVE 03/21/2014
HEART VALVES SANTA ANA MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 02/12/2014
-
-