• 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
STRYKER / HOWMEDICA OSTEONICS CORP STRYKER HIP REPLACEMENT 05/03/2024
STRYKER / HOWMEDICA OSTEONICS CORP. STRYKER HIP REPLACEMENT 05/03/2024
DEPUY ORTHOPAEDICS INC US PINNACLE 100 ACET CUP 54MM 05/03/2024
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +5 05/03/2024
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR CUP 05/02/2024
ZIMMER BIOMET, INC. G7 OSSEOTI ACETABULAR SHELL MULTI HOLE 5 05/02/2024
ZIMMER BIOMET, INC. G7 LONGEVITY NEUTRAL 36MM F 05/01/2024
ZIMMER MANUFACTURING B.V. BONE SCR 6.5X35 SELF-TAP 05/01/2024
ZIMMER TMT HEDROCEL SOLUTION TRIPOLAR 05/01/2024
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL SLEEVE 04/30/2024
-
-