• 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
 

 
 < 
 1 
 2 
 3 
 4 
 
 
40 records meeting your search criteria returned- Product Code: JDI Patient Problem: Renal Failure Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. E-POLY 40MM MAXROM LNR SZ25 08/08/2018
ZIMMER BIOMET, INC. UNKNOWN ZIMMER LINER 04/25/2018
ZIMMER BIOMET, INC. UNKNOWN ZIMMER FEMORAL HEAD 04/25/2018
ZIMMER BIOMET, INC. UNKNOWN HIP 10/17/2017
DEPUY ORTHOPAEDICS INC US S-ROM M HEAD 36MM +0 10/10/2017
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +1.5 09/19/2017
DEPUY ORTHOPAEDICS, INC. 1818910  UNKNOWN DEPUY ACETABULAR LINER 09/19/2017
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/+5 03/14/2017
BIOMET ORTHOPEDICS UNKNOWN HIP 05/20/2016
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 04/28/2014
-
-