• 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
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE 018 04/24/2024
BOSTON SCIENTIFIC CORPORATION COYOTE ES 04/23/2024
CORDIS US CORP. SABERX RADIANZ 04/23/2024
CORDIS US. CORP AVIATOR PLUS 04/23/2024
COVIDIEN EVERCROSS 035 04/23/2024
CORDIS US. CORP SABERX 04/23/2024
COOK INC ADVANCE 18 LP LOW PROFILE BALLOON CATHET 04/22/2024
COVIDIEN FORTREX 0.035 OTW PTA BALLOON CATHETER 04/19/2024
COVIDIEN NANOCROSS 0.14 OTW PTA DILATATION CATHET 04/19/2024
COVIDIEN NANOCROSS 0.14 OTW PTA DILATATION CATHET 04/19/2024
-
-