• 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 
 
 
16 records meeting your search criteria returned- Product Code: HSX Product Problem: Device Slipped Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONFORMIS, INC. IUNI G2 04/16/2015
STRYKER ORTHOPAEDICS-MAHWAH UNI-KNEE MOD. TIBIAL BEAR INS. 09/26/2014
CONFORMIS IUNI G2 07/02/2014
STRYKER ORTHOPAEDICS-MAHWAH SERIES I TIBIAL BEARING INSERT 07/02/2014
CONFORMIS IUNI G2 05/21/2014
CONFORMIS INI G2 02/28/2014
-
-