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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 
 
50 records meeting your search criteria returned- Product Code: JDI Patient Problem: Impaired Healing Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNK TM SHELL 54MM 12/07/2019
ZIMMER BIOMET, INC. UNKNOWN STEM 11/27/2019
ZIMMER BIOMET, INC. UNKNOWN HEAD 11/27/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/11/2019
ZIMMER BIOMET, INC. G7 NEU +5MM E1 LINER 40MM G 09/30/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL AUGMENT 09/09/2019
ZIMMER MANUFACTURING B.V. FEMORAL STEM 12/14 NECK TAPER STANDARD O 08/22/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/18/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/18/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 06/18/2019
-
-