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 
 > 
 
57 records meeting your search criteria returned- Product Code: NIO Product Problem: Detachment Of Device Component Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC - MAPLE GROVE EPIC¿ 06/30/2016
BOSTON SCIENTIFIC - MAPLE GROVE EPIC¿ VASCULAR 06/28/2016
BOSTON SCIENTIFIC CORPORATION EXPRESS LD ILLIAC/BILIARY STENT 06/10/2016
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 04/25/2016
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 03/23/2016
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 02/26/2016
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTAR VASCULAR AND BILIARY STENT SYST 12/22/2015
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 12/16/2015
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 12/03/2015
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG E-LUMINEXX VASCULAR STENT 12/02/2015
-
-