• 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 records meeting your search criteria returned- Product Code: JDG Patient Problem: Cyst(s) Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 06/27/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 06/27/2019
ZIMMER BIOMET, INC. UNKNOWN 38 ACETABULAR CUP 10/08/2018
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 45 05/16/2016
DEPUY ORTHOPAEDICS, INC. UNK FEMORAL STEM 05/10/2016
DEPUY INTERNATIONAL LTD 8010379 UNKNOWN DEPUY FEMORAL STEM 03/26/2015
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 51 11/26/2014
-
-