• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: LWR Product Problem: Reflux within Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC HEART VALVES DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 02/06/2023
MEDTRONIC HEART VALVES DIVISION HANCOCK II AORTIC BIOPROSTHETIC HEART VA 12/13/2022
MEDTRONIC HEART VALVES DIVISION MOSAIC ULTRA PORCINE HEART VALVE 11/25/2022
MEDTRONIC HEART VALVES DIVISION HANCOCK II AORTIC BIOPROSTHETIC HEART VA 10/03/2022
MEDTRONIC HEART VALVES DIVISION MEDTRONIC SURGICAL TISSUE VALVE 09/22/2022
MEDTRONIC HEART VALVES DIVISION MEDTRONIC SURGICAL TISSUE VALVE 09/22/2022
MEDTRONIC HEART VALVES DIVISION HANCOCK II MITRAL BIOPROSTHETIC HEART VA 09/15/2022
MEDTRONIC HEART VALVES DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 09/02/2022
MEDTRONIC HEART VALVES DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 09/02/2022
MEDTRONIC HEART VALVES DIVISION MOSAIC MITRAL BIOPROSTHETIC VALVE 07/23/2022
-
-