• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
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
BOSTON SCIENTIFIC CORPORATION PERIPHERAL ROTAWIRE AND WIRECLIP TORQUER 01/23/2024
UNKNOWN ROTAREX 01/23/2024
MEDTRONIC IRELAND TURBOHAWK PLUS 6FR 01/19/2024
UNKNOWN ROTAREX 01/19/2024
BOSTON SCIENTIFIC CORPORATION JETSTREAM XC ATHERECTOMY CATHETER 01/18/2024
MEDTRONIC IRELAND TURBOHAWK PLUS 6FR 01/18/2024
UNKNOWN ROTAREX 01/17/2024
STRAUB MEDICAL AG ROTAREX 01/11/2024
UNKNOWN ROTAREX 01/11/2024
CARDIOVASCULAR SYSTEMS, INC. (ABBOTT) DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 01/10/2024
-
-