• 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 
 > 
 
25 records meeting your search criteria returned- Product Code: FOZ Patient Problem: Failure of Implant Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECTON, DICKINSON AND COMPANY BD NEXIVA 12/13/2023
BECTON DICKSON INFUSION THERAPY SYSTEMS AUTOGUARD WINGED ANGIOCATHETER 12/12/2023
BECTON DICKSON INFUSION THERAPY SYSTEMS AUTOGUARD WINGED ANGIOCATHETER 12/12/2023
BD BD INSYTE AUTOGUARD BC 09/13/2023
BECTON, DICKINSON AND COMPANY BD INSYTE AUTOGUARD SHIELDED IV CATHETER 08/18/2023
BECTON, DICKINSON AND COMPANY NEXIVA 08/10/2023
ARROW INTERNATIONAL, INC. (SUBSIDIARY OF BLUE PLUS THREE-LUMEN CVC 08/04/2023
C.R. BARD, INC. POWERGLIDE PRO MIDLINE CATHETER 07/28/2023
Unknown Manufacturer CATHETER 07/12/2023
TELEFLEX MEDICAL ARROW 06/23/2023
-
-