• 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
 

 
 
 1 
 2 
 > 
 
18 records meeting your search criteria returned- Product Code: GXQ Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INTEGRA LIFESCIENCES CORPORATION DURAGEN 1X1 5 PACK DOMESTIC 03/13/2018
INTEGRA LIFESCIENCES CORPORATION DURAGEN 3X3 5 PACK CE 03/13/2018
INTEGRA LIFESCIENCES CORPORATION DURAGEN 2X2 5 PACK DOMESTIC 03/13/2018
MEDTRONIC NEUROSURGERY DUREPAIR DURA SUBSTITUTE 02/16/2018
AESCULAP AG LYOPLANT ONLAY 10.0X12.5CM 08/08/2016
INTEGRA LIFESCIENCES CORP DURAGEN PLUS DURAL REGENERATION MATRIX 3 04/25/2016
COLLAGEN MATRIX, INC. DURAMATRIX 02/24/2016
INTEGRA LIFESCIENCES CORPORATION DURAGEN SUTURABLE DURAL REGENERATION TEM 12/21/2015
INTEGRA LIFESCIENCES CORPORATION DURAGEN-UNKNOWN PRODUCT ID 12/17/2015
INTEGRA NEUROSCIENCES PR DURAGEN SUTURABLE DURAL REGENERATION TEM 11/12/2015
-
-