Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 5 
 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  AML SM STATURE 10.5MM 03/11/2019
DEPUY ORTHOPAEDICS INC US S-ROM*STM STD,36NK,16X11X150 03/07/2019
DEPUY ORTHOPAEDICS, INC. 1818910  ARTICULEZE M HEAD 36MM +5 03/05/2019
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ10 STD OFF 03/01/2019
DEPUY ORTHOPAEDICS INC US S-ROM*STM STD,30 NK,16X11X150 02/28/2019
DEPUY ORTHOPAEDICS INC US 12/14 ARTICUL 40MM M SPEC+1.5 02/18/2019
DEPUY ORTHOPAEDICS, INC. 1818910 12/14 ARTICUL 40MM M SPEC-2 02/18/2019
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 02/15/2019
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 02/15/2019
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 02/15/2019
-
-