• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
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. AMBIENT SUPER TURBOVAC 90 IFS 02/26/2021
ARTHROCARE CORP. RF12000 Q2 SRVC, CONTROLLER-ONLY PACKAGE 02/18/2021
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 02/17/2021
ARTHROCARE CORP. FA COBLATOR II CONTROLLER (120V) 02/16/2021
ARTHROCARE CORP. RF12000 Q2 SRVC, CONTROLLER-ONLY PACKAGE 02/12/2021
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 02/12/2021
ARTHROCARE CORP. WEREWOLF SRVC RF20000 CONTROLLER 02/11/2021
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 02/10/2021
ARTHROCARE CORP. FOOT CONTROL ASSEMBLY 02/09/2021
ARTHROCARE CORP. RF12000 Q2 SRVC, CONTROLLER-ONLY PACKAGE 02/09/2021
-
-