• 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 
 
 
21 records meeting your search criteria returned- Product Code: KXA Product Problem: Break Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US SPECIALIST*2 UNIVERSAL HANDLE 02/26/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 02/01/2018
SMITH & NEPHEW ORTHOPAEDICS LTD RESURFACING FEMORAL HEAD 08/22/2017
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN PRECISION FEMORAL TRIAL 03/14/2017
ZIMMER GMBH METASUL DUROM, COMPONENT FOR FEMUR, CEME 02/23/2017
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY UNIVERSAL STEM 05/23/2016
STRYKER CORMET HEAD/CUP 08/14/2015
DEPUY ORTHOPAEDICS, INC. UNKNOWN SROM 36+8MM STD NECK 06/25/2015
DEPUY IRELAND 9616671 UNKNOWN DEPUY SZ. 28 +5 FEMORAL HEAD 04/10/2015
DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN DEPUY AML FEMORAL HIP STEM 06/27/2014
-
-