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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
108 records meeting your search criteria returned- Product Code: LWR Product Problem: Material Too Rigid or Stiff Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA CANADA CORP MITROFLOW DLA AORTIC PERICARDIAL HEART V 12/03/2018
LIVANOVA CANADA CORP CROWN PRT PERICARDIAL HEART VALVE 11/26/2018
Unknown Manufacturer CROWN PRT PERICARDIAL HEART VALVE 10/25/2018
LIVANOVA CANDA CORP MITROFLOW LXA AORTIC PERICARDIAL HEART V 09/25/2018
LIVANOVA CANDA CORP MITROFLOW DLA AORTIC PERICARDIAL HEART V 09/24/2018
LIVANOVA CANADA CORP. MITROFLOW 12A AORTIC PERICARDIAL HEART V 07/03/2018
LIVANOVA CANADA CORP MITROFLOW DLA 06/22/2018
SORIN GROUP ITALIA S.R.L. PERCEVAL SUTURELESS AORTIC HEART VALVE 06/11/2018
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 05/15/2018
LIVANOVA CANADA CORP MITROFLOW LXA 05/15/2018
-
-