• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
145 records meeting your search criteria returned- Product Code: GEI Product Problem: Failure to Power Up Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORP. UNKN COBLATOR II SURGERY SYSTEM AND WAND 09/14/2020
ARTHROCARE CORP. WEREWOLF SRVC RF20000 CONTROLLER 09/09/2020
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 09/08/2020
ARTHROCARE CORP. FA COBLATOR II CONTROLLER (120V) 09/04/2020
ARTHROCARE CORP. RF8000E (120V) SRVC, CONTROLLER-ONLY PG 09/04/2020
ARTHROCARE CORP. WEREWOLF RF 20000 CONTROLLER 09/03/2020
ARTHROCARE CORP. FA COBLATOR II CONTROLLER (120V) 09/02/2020
ARTHROCARE CORP. WEREWOLF RF 20000 CONTROLLER 08/11/2020
SMITH & NEPHEW, INC. VULCAN GENERATOR CE MARK 08/09/2020
ARTHROCARE CORP. FA COBLATOR II CONTROLLER (120V) 08/05/2020
-
-