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 
 > 
 
58 records meeting your search criteria returned- Product Code: KXA Patient Problem: Weakness Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY FRANCE SAS - 3003895575 UNKNOWN HIP FEMORAL STEM 04/09/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/26/2020
DEPUY ORTHOPAEDICS INC US UNK HIP FEMORAL STEM SUMMIT 03/09/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 02/26/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 02/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 01/17/2020
DEPUY INTERNATIONAL LTD - 8010379 ADAPTER SLEEVES 12/14 +2 12/30/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 12/02/2019
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 11/06/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 09/27/2019
-
-