• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
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
US SURGICAL PUERTO RICO PROTACK 09/25/2023
US SURGICAL PUERTO RICO AUTO SUTURE 09/18/2023
COVIDIEN LP LLC NORTH HAVEN ENDO PEANUT 09/12/2023
US SURGICAL PUERTO RICO PROTACK 09/08/2023
COVIDIEN LP LLC NORTH HAVEN LAPRO-CLIP 09/01/2023
US SURGICAL PUERTO RICO SPACEMAKER 09/01/2023
US SURGICAL PUERTO RICO SPACEMAKER 09/01/2023
US SURGICAL PUERTO RICO AUTO SUTURE 08/30/2023
INTUITIVE SURGICAL, INC NONE 08/28/2023
US SURGICAL PUERTO RICO UNKNOWN PROTACK 08/28/2023
-
-