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
 

 
 
10 records meeting your search criteria returned- Product Code: JDG Patient Problem: Death Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. HIP IMPLANT 10/28/2019
DEPUY ORTHOPAEDICS, INC. 1818910  UNKNOWN HIP FEMORAL STEM 02/12/2019
DEPUY ORTHOPAEDICS, INC. 1818910  UNKNOWN HIP FEMORAL HEAD 02/12/2019
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 47 02/06/2019
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL AUGMENT 12/04/2018
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN REJUVENATE STEM 04/26/2018
BIOMET UK LTD. UNKNOWN FEMORAL HEAD 07/14/2017
BIOMET ORTHOPEDICS UNKNOWN LINER 07/12/2017
BIOMET ORTHOPEDICS UNKNOWN HEAD 07/12/2017
DEPUY INTL., LTD. - 8010379 UNIDENTIFIED ASR HEAD 05/21/2015
-
-