• 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
 

 
 
9 records meeting your search criteria returned- Product Code: GXN Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PSI SD800.426 PEEK IMPLANT 06/11/2018
AESCULAP AG CRANIOFIX 2 APPLYING FORCEPS NON-DETACH 05/01/2018
AESCULAP IMPLANT SYSTEMS CRANIOFIX 2 TITANIUM CLAMP 20MM 04/24/2018
AESCULAP IMPLANT SYSTEMS CRANIOFIX 2 TITANIUM CLAMP 20MM 04/24/2018
AESCULAP IMPLANT SYSTEMS CRANIOFIX 2 TITANIUM CLAMP 20MM 04/24/2018
OXFORD PERFORMANCE MATERIALS HTR-PEKK 02/14/2018
AESCULAP AG CRANIOFIX 2 APPLYING FORCEPS NON-DETACH 10/12/2017
OXFORD PERFORMANCE MATERIALS, INC. HTR-PEKK 01/19/2017
SYNTHES USA PLATE, CRANIOPLASTY, PREFORMED, NONALTER 01/13/2017
-
-