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 
 7 
 8 
 9 
 10 
 > 
 
109 records meeting your search criteria returned- Product Code: NIO Patient Problem: Reocclusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ZILVER PTX 35 DRUG-ELUTING STENT 02/18/2021
MEDTRONIC IRELAND COMPLETE SE ILIAC 09/17/2020
COVIDIEN VISI-PRO BALLOON-EXPANDABLE STENT SYSTEM 09/02/2020
COVIDIEN VISI-PRO BALLOON-EXPANDABLE STENT SYSTEM 06/12/2020
COVIDIEN VISI-PRO BALLOON-EXPANDABLE STENT SYSTEM 06/12/2020
MEDTRONIC IRELAND COMPLETE SE ILIAC 03/06/2020
BOSTON SCIENTIFIC CORPORATION EPIC 07/17/2019
MEDTRONIC IRELAND COMPLETE SE ILIAC 05/10/2019
COVIDIEN PROTEGE GPS SELF-EXPANDING STENT SYSTEM 05/09/2019
COVIDIEN PROTEGE GPS SELF-EXPANDING STENT SYSTEM 05/09/2019
-
-