• 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
 

 
 
 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, BRASIL LTDA. (PAMPULHA SJM TRIFECTA VALVE 08/03/2020
EDWARDS LIFESCIENCES EDWARDS INTUITY ELITE VALVE SYSTEM 07/31/2020
ST. JUDE MEDICAL, INC. (CS-WOODRIDGE) TRIFECTA GT VALVE 07/21/2020
ST. JUDE MEDICAL SJM TRIFECTA VALVE 04/13/2020
LIVANOVA CANADA CORP PERCEVAL SUTURELESS AORTIC HEART VALVE 12/24/2019
LIVANOVA CANADA CORP PERCEVAL SUTURELESS AORTIC HEART VALVE 12/24/2019
MEDTRONIC HEART VALVE DIVISION HANCOCK II AORTIC BIOPROSTHETIC HEART VA 11/22/2019
SORIN GROUP ITALIA S.R.L. PERCEVAL SUTURELESS AORTIC HEART VALVE 10/21/2019
SORIN GROUP ITALIA S.R.L. PERCEVAL SUTURELESS AORTIC HEART VALVE 10/21/2019
EDWARDS LIFESCIENCES EDWARDS INTUITY ELITE VALVE SYSTEM 09/13/2019
-
-