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 
 3 
 > 
 
22 records meeting your search criteria returned- Product Code: GXN Patient Problem: Failure of Implant Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.440 PEEK IMPLANT 01/05/2021
SYNTHES GMBH PATIENT SPECIFIC IMPLANT PEEK/ EXPRESS 12/24/2020
SYNTHES GMBH PATIENT SPECIFIC IMPLANT PEEK/ EXPRESS 12/23/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.401 PEEK IMPLANT 12/08/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.440 PEEK IMPLANT 11/10/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.427 PEEK IMPLANT 10/06/2020
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.401 PEEK IMPLANT 08/06/2020
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.440 PEEK IMPLANT 02/05/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD420.526 TITANIUM IMPLANT 01/13/2020
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - PSI IMPLANTS 12/20/2019
-
-