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

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
 

 
 
 1 
 2 
 > 
 
16 records meeting your search criteria returned- Product Code: PFO Product Problem: Loss of Osseointegration Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COCHLEAR LIMITED COCHLEAR OSIA OSI200 IMPLANT 10/23/2023
COCHLEAR LIMITED COCHLEAR OSIA OSI200 IMPLANT 10/23/2023
COCHLEAR LTD COCHLEAR OSIA OSI200 IMPLANT 06/26/2023
COCHLEAR LTD COCHLEAR OSIA OSI200 IMPLANT 06/26/2023
COCHLEAR LTD COCHLEAR OSIA OSI200 IMPLANT 05/29/2023
COCHLEAR LIMITED COCHLEAR OSIA OSI200 IMPLANT 05/29/2023
COCHLEAR LIMITED COCHLEAR OSIA OSI200 IMPLANT 03/13/2023
COCHLEAR BONE ANCHORED SOLUTIONS AB COCHLEAR OSIA OSI200 IMPLANT 01/29/2023
COCHLEAR LIMITED COCHLEAR OSIA OSI200 IMPLANT 01/29/2023
COCHLEAR LTD COCHLEAR OSIA OSI200 IMPLANT 02/17/2022
-
-