• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
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
BIOMET FRANCE S.A.R.L. VARIZED FEMORAL STEM EXCEPTION RIGHT SIZ 12/09/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 12/08/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 12/08/2020
SMITH & NEPHEW, INC. TANDEM BIPOLAR COCR 46OD 28ID 12/08/2020
DEPUY ORTHOPAEDICS INC US UNK HIP FEMORAL STEM SUMMIT 12/08/2020
DEPUY ORTHOPAEDICS INC US SELF CENT HIP 52X28 BLU 12/07/2020
BIOMET UK LTD. UNKNOWN CEMENTED UKR 12/07/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 12/07/2020
ORTHO DEVELOPMENT ENCOMPASS HIP STEM 12/07/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR CUP 12/06/2020
-
-