• 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 
 4 
 5 
 6 
 > 
 
60 records meeting your search criteria returned- Product Code: GXN Product Problem: Defective Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH PSI SD800.535 PEEK IMPLANT 12/21/2023
SYNTHES GMBH PSI SD800.434 PEEK IMPLANT 09/27/2023
SYNTHES GMBH PSI SD800.420 PEEK IMPLANT 09/19/2023
SYNTHES GMBH PSI 140*100*40 PEEK 07/31/2023
SYNTHES GMBH PSI SD800.434 PEEK IMPLANT 07/25/2023
SYNTHES GMBH PSI SD800.402 PEEK IMPLANT 04/17/2023
SYNTHES GMBH PSI SD800.433 PEEK IMPLANT 03/02/2023
SYNTHES GMBH PSI SD800.510 PEEK IMPLANT 01/30/2023
SYNTHES GMBH CUSTOM-MADE DEVICE TRUMATCH CMF PEEK MIL 01/19/2023
SYNTHES GMBH PSI 140*120*40 PEEK 12/23/2022
-
-