• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
125 records meeting your search criteria returned- Product Code: JDI Patient Problem: Swelling Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +5 02/06/2019
DEPUY ORTHOPAEDICS, INC. 1818910  12/14 ARTICUL 40MM M SPEC+1.5 02/06/2019
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +5 02/06/2019
DEPUY ORTHOPAEDICS, INC. 1818910 12/14 ARTICUL 40MM M SPEC+1.5 02/06/2019
DEPUY ORTHOPAEDICS INC US PINN 100 W/GRIPTION 58MM 02/05/2019
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM -2 02/04/2019
DEPUY IRELAND - 9616671 SROM*STM ST,36+8L NK,18X13X160 01/30/2019
DEPUY ORTHOPAEDICS INC US TC3 RP TIBIAL INSERT S5,17.5 01/30/2019
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN STRYKER HIP 01/30/2019
DEPUY ORTHOPAEDICS INC US AML LG STATURE 16.5MM 01/28/2019
-
-