• 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
 

 
 
6 records meeting your search criteria returned- Product Code: KXA Product Problem: Loosening of Implant Not Related to Bone-Ingrowth Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. CONSERVE FEMORAL RESURFACING HEAD 44MM 12/31/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 04/27/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 04/27/2020
ZIMMER SWITZERLAND MANUFACTURING GMBH REVITAN, DISTAL PART, STRAIGHT, UNCEMENT 03/26/2020
DEPUY INTERNATIONAL LTD - 8010379 TOTAL ASR FEM IMP SIZE 46 02/24/2020
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 08/09/2019
-
-