• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
 
85 records meeting your search criteria returned- Product Code: LWR Patient Problem: Insufficiency, Valvular Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, COSTA RICA LTDA (SH) TRIFECTA GT VALVE 11/09/2020
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 10/22/2020
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 10/22/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (SH) TRIFECTA GT VALVE 10/13/2020
MEDTRONIC HEART VALVES DIVISION MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 10/07/2020
ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA SJM TRIFECTA VALVE 10/05/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) TRIFECTA GT VALVE 09/22/2020
MEDTRONIC HEART VALVES DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 09/02/2020
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) TRIFECTA STENTED TISSUE VALVE 08/20/2020
MEDTRONIC HEART VALVE DIVISION HANCOCK II AORTIC CINCH 23 07/10/2020
-
-