• 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
 

 
 
6 records meeting your search criteria returned- Product Code: KWD Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
VILEX, LLC CHI 01/30/2024
BIOPOLY LLC BIOPOLY GREAT TOE HEMIARTHROPLASTY IMPLA 10/09/2023
BIOPOLY LLC BIOPOLY GREAT TOE HEMIARTHROPLASTY IMPLA 04/24/2023
VILEX IN TENNESSEE, INC. VILEX HEMI IMPLANT 02/27/2018
ASCENSION ORTHOPEDICS MGT MOVEMENT PROX. PHAL. TOTAL SZ. 40 01/13/2016
WRIGHT MEDICAL TECHNOLOGY, INC. LPT GREAT TOE IMPLANT 07/24/2015
-
-