• 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 
 > 
 
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
MEDOS INTERNATIONAL SARL PROWLER SELECT PLUS 150/5CM 12/29/2023
MEDOS INTERNATIONAL SARL PROWLER SELECT PLUS 150/5CM 12/28/2023
BOSTON SCIENTIFIC CORPORATION EKOSONIC ENDOVASCULAR DEVICE, 106X12CM 12/22/2023
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 12/22/2023
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 12/22/2023
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 12/22/2023
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 12/22/2023
BOSTON SCIENTIFIC CORPORATION EKOS ENDOVASCULAR DEVICE, 106X18CM 12/22/2023
BOSTON SCIENTIFIC CORPORATION DIREXION TRANSEND-14 SYSTEM 12/21/2023
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 12/21/2023
-
-