• 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 
 11 
 12 
 > 
 
118 records meeting your search criteria returned- Product Code: GEX Product Problem: No Apparent Adverse Event Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DORNIER MEDTECH AMERICA, INC. DORNIER HOLMIUM LASER FIBER 06/16/2020
MONTERIS MEDICAL NEUROBLATE SYSTEM 05/17/2020
DORNIER MEDTECH AMERICA, INC. DORNIER HOLMIUM LASER FIBER 05/14/2020
DORNIER MEDTECH AMERICA, INC. DORNIER HOLMIUM LASER FIBER 04/09/2020
DORNIER MEDTECH AMERICA, INC. DORNIER HOLMIUM LASER FIBER 02/03/2020
MONTERIS MEDICAL NEUROBLATE® SYSTEM 01/17/2020
DORNIER MEDTECH SYSTEMS GMBH DORNIER DIODE LASER FIBER 01/16/2020
QUANTA SYSTEM S.P.A. OLYMPUS EMPOWER H65 01/10/2020
DORNIER MEDTECH SYSTEMS GMBH DORNIER DIODE LASER FIBER 11/22/2019
MONTERIS MEDICAL NEUROBLATE® SYSTEM 11/13/2019
-
-