• 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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
153 records meeting your search criteria returned- Product Code: KXA Product Problem: Corroded Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 51 12/22/2014
DEPUY INTL., LTD. - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 12/11/2014
DEPUY ORTHOPAEDICS, INC. - 1818910 UNKNOWN DEPUY FEMORAL STEM 12/11/2014
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY FEMORAL STEM 12/02/2014
DEPUY ORTHOPAEDICS, INC. - 1818910 UNKNOWN DEPUY FEMORAL STEM 12/02/2014
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY FEMORAL STEM 11/04/2014
DEPUY INTL., LTD. - 8010379 UNKNOWN DEPUY ASR SLEEVE SIZE -2 09/17/2014
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 53 09/05/2014
DEPUY INTL., LTD. - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 07/21/2014
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY HIP STEM 07/15/2014
-
-