Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
129 records meeting your search criteria returned- Product Code: GEI Product Problem: No Device Output Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC ADVANCED ENERGY (SALIENT) PLASMABLADE 3.0S 06/02/2021
GYRUS ACMI, INC GYRUS, PK-SP GENERATOR 06/01/2021
ARTHROCARE CORP. QUANTUM 2 CONTROLLER 05/25/2021
GYRUS ACMI, INC MULTIDEBRIDER HANDPIECE, ANGLED 05/04/2021
MEDTRONIC ADVANCED ENERGY (SALIENT) PLASMABLADE 4.0 04/30/2021
MEDTRONIC INC. / COVIDIEN LIGASURE MARYLAND JAW LAPAROSCOPIC SEALE 04/30/2021
SMITH NEPHEW, INC. COBLATION 04/28/2021
COVIDIEN FORCETRIAD 04/21/2021
GYRUS ACMI, INC MULTIDEBRIDER HANDPIECE, ANGLED 04/05/2021
MEDTRONIC ADVANCED ENERGY (SALIENT) PLASMABLADE X 03/15/2021
-
-