• 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
 

 
 < 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 19 
 20 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE 035 PTA DILATATION CATHETER 03/19/2021
BIOTRONIK AG, BUELACH, SWITZERLAND PASSEO-14 2.5/140/150 03/11/2021
MEDTRONIC MEXICO ADMIRAL XTREME OTW 03/08/2021
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE RX PTA DILATATION CATHETER 03/05/2021
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 02/24/2021
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 02/08/2021
ABBOTT VASCULAR RX VIATRAC 14 PLUS PERIPHERAL DILATATION 01/13/2021
BOSTON SCIENTIFIC CORPORATION 2CM PERIPHERAL CUTTING BALLOON 01/08/2021
COVIDIEN NANOCROSS ELITE 0.14 OTW PTA DILATATION 01/04/2021
COVIDIEN NANOCROSS ELITE 0.14 OTW PTA DILATATION 12/29/2020
-
-