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 
 > 
 
53 records meeting your search criteria returned- Product Code: NIO Product Problem: Device Damaged by Another Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 09/15/2015
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 08/13/2015
BOSTON SCIENTIFIC - MAPLE GROVE EPIC? VASCULAR 04/23/2015
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 03/06/2015
BOSTON SCIENTIFIC - GALWAY EXPRESS LD ILIAC/BILIARY PREMOUNTED STEN 01/08/2015
BOSTON SCIENTIFIC - MAPLE GROVE EPIC? VASCULAR 11/24/2014
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 11/14/2014
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 10/14/2014
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 07/01/2014
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 05/29/2014
-
-