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
 

 
 
7 records meeting your search criteria returned- Product Code: KWD Report Date From: 1/1/2016 Report Date To: 12/31/2016

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER GMBH UNKNOWN SMART TOE IMPLANT 10/18/2016
VILEX, INC. MINI MET HEAD 09/01/2016
VILEX, INC. VILEX HEMI IMPLANT 05/27/2016
ARTHROSURFACE, INC. CAP GREAT TOE RESURFACING HEMI-ARTHROPLA 04/06/2016
VILEX, INC. VILEX MINI METHEAD 03/17/2016
VILEX, INC. VILEX MINI MET HEAD 01/20/2016
ASCENSION ORTHOPEDICS MGT MOVEMENT PROX. PHAL. TOTAL SZ. 40 01/13/2016
-
-