• 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 
 > 
 
46 records meeting your search criteria returned- Product Code: KXA Product Problem: Loose or Intermittent Connection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 45 08/13/2014
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 08/13/2014
BIOMET ORTHOPEDICS RECAP PF FMRL HD RESURF 54MM 07/18/2014
BIOMET ORTHOPEDICS RECAP PF FMRL HD RESURF 52MM 07/17/2014
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 52M 07/09/2014
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 50M 07/09/2014
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 52M 07/08/2014
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 58M 07/08/2014
BIOMET ORTHOPEDICS RECAP CEMENTED FEMORAL HEAD RESURFACING 07/07/2014
HOWMEDICA/OSTEONIC FEMORAL HEAD LOW FRICTION ION TREATMENT 06/06/2014
-
-