• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
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
SMITHS MEDICAL ASD, INC. BIVONA 02/23/2022
NULL BLUPERC AND BLUGRIGGS PERCUTANEOUS DILAT 02/18/2022
SMITHS MEDICAL ASD, INC. BIVONA TUBES NEO/PED FLEXTEND 02/03/2022
NULL BIVONA TRACHEOSTOMY TUBE, ADULT? 01/31/2022
COVIDIEN SHILEY 8.0 01/21/2022
COVIDIEN SHILEY 7.0 01/21/2022
NULL TRACHEOSTOMY TUBE 01/07/2022
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 01/07/2022
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 01/07/2022
SMITHS MEDICAL ASD, INC. BIVONA 01/06/2022
-
-