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 03/06/2017
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 01/19/2017
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 12/20/2016
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 12/15/2016
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 12/15/2016
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 11/23/2016
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 08/05/2016
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 05/23/2016
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 09/21/2015
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 09/15/2015
-
-