• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
9 records meeting your search criteria returned- Product Code: HSX Product Problem: Malposition of Device Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP IMPLANT SYSTEMS LLC / B. BRAUN TOTAL KNEE REPLACEMENT 10/17/2018
MAKO SURGICAL CORP. UNKNOWN MAKO BASEPLATE 08/31/2018
MAKO SURGICAL CORP. UNKNOWN MAKO FEMORAL COMPONENT 08/31/2018
ZIMMER BIOMET, INC. ZIMMER UNI FIXED TIBIAL PLATE 05/24/2018
CONFORMIS, INC. IUNI G2 11/08/2017
MAKO SURGICAL CORP. UNKNOWN RESTORIS SZ 4 RIGHT MEDIAL TIBIA 10/31/2017
MAKO SURGICAL CORP. UNKNOWN RESTORIS SZ 3 RIGHT MEDIAL FEMOR 10/31/2017
ZIMMER, INC. ZIMMER UNICOMPARTMENTAL KNEE ARTICULAR S 10/05/2016
CONFORMIS, INC. IUNI G2 12/10/2015
-
-