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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
257 records meeting your search criteria returned- Product Code: KXA Product Problem: Metal Shedding Debris Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN ASR FEMORAL HEAD 10/08/2015
BIOMET UK LTD. RECAP FEM HEAD COCR CEMENTED DIA44MM 10/02/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SF W/HM TECH. FEMORAL COMPON 08/21/2015
DEPUY INTL.,LTD 8010379 UNKNOWN DEPUY ASR HEAD 08/04/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 05/28/2015
BIOMET UK LTD. RECAP FEMORAL HEAD COCR CEMENTED DIA42MM 05/28/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 05/19/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SF W/HM TECH. FEMORAL COMPON 05/18/2015
DEPUY INTERNATIONAL LTD. - 8010379 UNKNOWN DEPUY ASR FEMORAL HEAD 05/14/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 04/29/2015
-
-