• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: GXN Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.401 PEEK IMPLANT 10/30/2020
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.402 PEEK IMPLANT 10/16/2020
OXFORD PERFORMANCE MATERIALS HTR-PEKK 03/05/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.541 PEEK IMPLANT 10/17/2019
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.540 PEEK IMPLANT 07/17/2019
BIOMET MICROFIXATION RAPIDFLAP (TM) SYSTEM 16 MM RAPIDFLAP SP 01/09/2019
OSSDSIGN OSSDSIGN CRANIAL PSI 12/19/2018
KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. IPS 11/30/2018
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.428 PEEK IMPLANT 10/25/2018
OBERDORF SYNTHES PRODUKTIONS GMBH PSI SD800.440 PEEK IMPLANT 05/11/2018
-
-