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

MAUDE - Manufacturer and User Facility Device Experience
  • 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
71 records meeting your search criteria returned- Product Code: KXA Product Problem: Loss of or Failure to Bond Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 04/27/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 04/27/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/19/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL STEM 02/21/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 02/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/31/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/17/2020
DEPUY FRANCE SAS - 3003895575 CORAIL CEM STEM STD S12 01/06/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 12/05/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 12/05/2019
-
-