• 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 
 
 
11 records meeting your search criteria returned- Product Code: HSN Patient Problem: Tissue Damage Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TIBIAL TRAY 01/03/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TIBIAL INSERT 01/03/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TALAR 01/03/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE IMPLANT 10/07/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE IMPLANT 10/07/2019
ZIMMER BIOMET, INC. TALAR COMPONENT 09/02/2019
ZIMMER BIOMET, INC. TIBIAL BASE COMPONENT 09/02/2019
ZIMMER BIOMET, INC. TIBIAL INSERT COMPONENT 09/02/2019
WRIGHT MEDICAL TECHNOLOGY, INC. INFINITY® TALAR DOME SZ 2 TOTAL ANKLE SY 01/17/2017
INTEGRA LIFESCIENCES CORPORATION OH/USA CADENCE IMPLANT-UNSPECIFIED 12/20/2016
-
-