• 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 
 > 
 
16 records meeting your search criteria returned- Product Code: NIO Product Problem: Kinked Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 06/11/2018
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 04/23/2018
BOSTON SCIENTIFIC - MAPLE GROVE EPIC¿ 11/10/2017
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTAR VASCULAR STENT SYSTEM 09/06/2017
COOK IRELAND LTD ZILVER FLEX 35 VASCULAR SELF-EXPANDING S 08/11/2017
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 10/18/2016
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 07/25/2016
BOSTON SCIENTIFIC - MAPLE GROVE EPIC¿ 05/25/2016
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 05/11/2016
COOK IRELAND LTD ZILVER FLEX 35 VASCULAR SELF-EXPANDING S 01/12/2016
-
-