• 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 
 > 
 
32 records meeting your search criteria returned- Product Code: FGE Product Problem: Material Frayed Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION SES SMART CONTROL 10X80 80 08/14/2019
BARD PERIPHERAL VASCULAR, INC. NAVARRE PERCUTANEOUS BILIARY DRAINAGE CA 05/07/2018
COOK INCORPORATED FUSION QUATTRO 04/23/2018
CORDIS CORPORATION SMART 120 150, SFA - 6X150MM 11/15/2017
COOK COOK MEDICAL 10/19/2016
CORDIS CORPORATION S.M.A.R.T. NITINOL STENT SYSTEM 08/16/2016
CORDIS CORPORATION PALMAZ GENESIS ON AMIIA 07/25/2016
CORDIS CORPORATION S.M.A.R.T. NITINOL STENT SYSTEM 06/22/2016
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 02/25/2016
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 02/22/2016
-
-