• 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
 

 
 < 
 1 
 2 
 
 
20 records meeting your search criteria returned- Product Code: LWR Patient Problem: Syncope Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, COSTA RICA LTDA EPIC STENTED PORCINE HEART VALVE W/FLEXF 08/15/2019
LIVANOVA CANADA CORP PERCEVAL SUTURELESS AORTIC HEART VALVE 02/11/2019
MEDTRONIC HEART VALVE DIVISION HANCOCK II AORTIC BIOPROSTHETIC HEART VA 04/23/2018
SORIN GROUP ITALIA S.R.L. PERCEVAL SUTURELESS AORTIC HEART VALVE 12/08/2017
MEDTRONIC HEART VALVES DIVISION MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 12/17/2015
ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA EPIC SUPRA VALVE W/FLEXFIT 06/17/2015
MEDTRONIC HEART VALVES DIVISION MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 05/20/2015
SORIN GROUP CANADA INC. MITROFLOW AORTIC PERICARDIAL HEART VALVE 08/19/2014
ST JUDE MEDICAL BRASIL LTDA SJM EPIC STENTED PORCINE HEART VALVE 04/18/2014
ST JUDE MEDICAL SJM EPIC STENTED PORCINE HEART VALVE 02/21/2014
-
-