• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
97 records meeting your search criteria returned- Product Code: GXN Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG & CO KG CRANIOFIX 2 TITANIUM CLAMP 16MM 03/09/2015
SYNTHES BRANDYWINE PSI SD800.533 PEEK IMPLANT 03/09/2015
SYNTHES BRANDYWINE PSI SD800.441 PEEK IMPLANT 02/10/2015
SYNTHES MEZZOVICO PSI SD800.428 PEEK IMPLANT 12/22/2014
SYNTHES BRANDYWINE PSI SD800.427 PEEK IMPLANT 12/19/2014
SYNTHES BRANDYWINE PSI SD800.510 PEEK IMPLANT 12/19/2014
SYNTHES BRANDYWINE PSI SD800.410 PEEK IMPLANT 12/19/2014
AESCULAP AG & CO KG. CRANIOFIX 2 TITANIUM CLAMP 16MM 10/02/2014
SYNTHES BRANDYWINE PSI SD800.441 PEEK IMPLANT 07/29/2014
SYNTHES (USA) TI CRANIAL FLAP TUBE CLAMP 13MM DIA 06/26/2014
-
-