• 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
 

 
 
10 records meeting your search criteria returned- Product Code: KWD Report Date From: 1/1/2017 Report Date To: 12/31/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 12/26/2017
ARTHREX INC. ANATOEMIC, 18.5MM 11/21/2017
VILEX IN TENNESSEE, INC. VILEX IMPLANT 11/15/2017
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 10/25/2017
ARTHROSURFACE, INC. CAP GREAT TOE RESURFACING HEMI-ARTHROPLA 10/17/2017
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 09/14/2017
ARTHROSURFACE, INC. CAP - GREAT TOE RESURFACING HEMI-ARTHROP 08/22/2017
ARTHROSURFACE, INC. CAP GREAT TOE RESURFACING HEMI-ARTHROPLA 05/24/2017
ARTHROSURFACE, INC. CAP GREAT TOE RESURFACING HEMI-ARTHROPLA 05/24/2017
TORNIER INC. PROTHESIS, TOE, HEMI- PHALANGEAL UNIVERS 04/11/2017
-
-