• 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: FZE Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/14/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/14/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/13/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/13/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/13/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB NI 06/13/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB COCHLEAR¿ VISTAFIX® VXA300 ABUTMENT 4.5M 06/22/2022
COCHLEAR BONE ANCHORED SOLUTIONS AB COCHLEAR¿ VISTAFIX® VXA300 ABUTMENT 4.5M 06/22/2022
COCHLEAR BONE ANCHORED SOLUTIONS AB COCHLEAR VISTAFIX VXI300 IMPLANT 4MM 04/07/2021
-
-