• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
25 records meeting your search criteria returned- Product Code: DXE Product Problem: Defective Device Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAYER HEALTHCARE LLC SPIROFLEX 05/19/2023
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 05/02/2023
EDWARDS LIFESCIENCES LLC FOGARTY 01/12/2023
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 01/10/2023
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 01/04/2023
BOSTON SCIENTIFIC CORPORATION SPIROFLEX ANGIOJET THROMBECTOMY SET 05/11/2022
BOSTON SCIENTIFIC CORPORATION ANGIOJET¿ SOLENT¿ OMNI 02/07/2022
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 12/21/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 12/21/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 10/13/2021
-
-