• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
257 records meeting your search criteria returned- Product Code: KXA Product Problem: Metal Shedding Debris Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD.-8010379 DEPUY ASR FEM IMPLANT SZ 51 04/22/2015
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 04/20/2015
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 53 04/09/2015
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 03/30/2015
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 52M 03/26/2015
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY FEMORAL STEM 03/16/2015
DEPUY ORTHOPAEDICS, INC. 1818910 SROM*STM ST,36+8L NK,20X15X165 03/14/2015
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR46MM 03/06/2015
DEPUY INTL., LTD. - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 03/03/2015
DEPUY INTL., LTD. - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 02/16/2015
-
-