Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 01/10/2018
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 01/10/2018
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 01/10/2018
DEPUY INT'L LTD. 8010379 UNKNOWN HIP FEMORAL AUGMENT 01/09/2018
DEPUY INT'L LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 01/09/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR ACETABULAR CUP 01/04/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 01/04/2018
DEPUY ORTHOPAEDICS, INC. 1818910  ASPHERE M SPEC 12/14 36 +1.5 01/04/2018
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL STEM 12/14/2017
DEPUY INTERNATIONAL LTD - 8010379 DEPUY ASR FEM IMPLANT SZ 47 12/14/2017
-
-