• 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
 

 
 < 
 6 
 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. 1818910 SROM STM STD 36+12L 15X20 02/14/2019
STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO. HIP REPLACEMENT 02/12/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 02/08/2019
DEPUY ORTHOPAEDICS INC US ASPHERE M SPEC 12/14 40 +1.5 02/08/2019
DEPUY ORTHOPAEDICS INC US 12/14 ARTICUL 40MM M SPEC+15.5 02/08/2019
DEPUY ORTHOPAEDICS INC US SROM*STM ST,30+4L NK,16X11X150 02/08/2019
DEPUY ORTHOPAEDICS, INC. 1818910 TC3 RP TIBIAL INSERT S5,17.5 02/07/2019
DEPUY ORTHOPAEDICS INC US S-ROM M HEAD 36MM +0 02/06/2019
DEPUY ORTHOPAEDICS INC US S-ROM M HEAD 36MM +6 02/06/2019
DEPUY INTERNATIONAL LTD. 8010379 ARTICUL/EZE BALL 32 +5 BR 02/06/2019
-
-