• 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 
 > 
 
46 records meeting your search criteria returned- Product Code: HSX Product Problem: Loose or Intermittent Connection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONFORMIS, INC. IUNI G2 01/10/2018
SMITH & NEPHEW, INC. JOURNEY UNI TIB BASE LM/RL SZ 3 06/15/2017
SMITH & NEPHEW, INC. ACCURIS UNI KNEE SYSTEM 12/16/2016
CONFORMIS, INC. IUNI G2 08/24/2016
CONFORMIS, INC. IUNI G2 08/01/2016
CONFORMIS, INC. IUNI 06/08/2016
CONFORMIS, INC IUNI G2 04/19/2016
SMITH & NEPHEW, INC. JOURNEY UNI TIB BASE RM/LL SZ 5 11/24/2015
CONFORMIS, INC. IUNI G2 10/21/2015
STRYKER ORTHOPAEDICS-MAHWAH UNI-KNEE TIBIAL COMPONENT 09/26/2014
-
-