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
 

 
 
7 records meeting your search criteria returned- Product Code: DXE Patient Problem: No Code Available Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. INDIGO SYSTEM CAT3 ASPIRATION CATHETER 08/11/2020
PENUMBRA, INC. INDIGO SYSTEM CAT5 ASPIRATION CATHETER 08/11/2020
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 08/11/2020
MEDOS INTERNATIONAL SARL REVIVE SE 4.5MM OUS 05/27/2020
EDWARDS LIFESCIENCES, PR FOGARTY ARTERIAL EMBOLECTOMY CATHETER 02/10/2020
EDWARDS LIFESCIENCES LLC FOGARTY ARTERIAL EMBOLECTOMY 10/01/2019
LEMAITRE VASCULAR, INC. OVER-THE-WIRE EMBOLECTOMY CATHETER 04/05/2019
-
-