• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
159 records meeting your search criteria returned- Product Code: JDI Patient Problem: Deformity/ Disfigurement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +1.5 10/18/2018
DEPUY ORTHOPAEDIC INC, 1818910 AML SM STATURE 18.0MM 10/18/2018
DEPUY ORTHOPAEDICS INC 1818910 ASPHERE M SPEC 12/14 40 +1.5 10/18/2018
DEPUY ORTHOPAEDIC INC, 1818910 12/14 ARTICUL 40MM M SPEC+1.5 10/18/2018
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ7 HI OFF 10/18/2018
DEPUY FRANCE SAS 3003895575 ARTICULEZE M HEAD 36MM +1.5 10/11/2018
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +5 10/05/2018
DEPUY ORTHOPAEDICS, INC. 1818910 ARTICULEZE M HEAD 36MM +1.5 09/27/2018
DEPUY ORTHOPAEDICS INC US 12/14 ARTICUL 40MM M SPEC+12 09/24/2018
DEPUY ORTHOPAEDICS, INC. 1818910 SUMMIT CEMENTED STEM SZ5 STD 09/21/2018
-
-