• 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
COOK INC GUNTHER TULIP FEMORAL VENA CAVA FILTER S 01/25/2024
COOK INC GUNTHER TULIP JUGULAR VENA CAVA FILTER S 12/07/2023
COOK INC UNKNOWN 10/31/2023
WILLIAM COOK EUROPE UNKNOWN 09/12/2023
WILLIAM COOK EUROPE UNKNOWN 07/26/2023
COOK INC UNKNOWN 06/13/2023
WILLIAM COOK EUROPE COOK CELECT NAVALIGN FEMORAL VENA CAVA F 05/26/2023
WILLIAM COOK EUROPE UNKNOWN 04/28/2023
WILLIAM COOK EUROPE UNKNOWN 04/18/2023
COOK INC GUNTHER TULIP FEMORAL VENA CAVA FILTER S 04/11/2023
-
-