• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
187 records meeting your search criteria returned- Product Code: GEI Product Problem: Failure to Shut Off Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORPORATION WEREWOLF FLOW 90 COBLATION WAND 12/12/2022
ARTHROCARE CORPORATION WEREWOLF FLOW 90 COBLATION WAND 12/08/2022
ARTHROCARE CORP. WEREWOLF FASTSEAL 6.0 11/08/2022
ARTHROCARE CORP. AMBIENT SUPER TURBOVAC 90 IFS 09/23/2022
ARTHROCARE CORP. WEREWOLF FLOW 50 COBLATION WAND 09/03/2022
MEDTRONIC ADVANCED ENERGY (SALIENT) AQUAMANTYS SBS 5.0 08/31/2022
STRYKER ENDOSCOPY-SAN JOSE SERFAS ENERGY 90-S CRUISE 08/18/2022
ARTHROCARE CORP. WEREWOLF FLOW 90 COBLATION WAND 07/18/2022
MEDTRONIC, INC. PS210-030S-LIGHT 06/30/2022
STRYKER ENDOSCOPY-SAN JOSE RF 2 PROBES, MICRO-CLAW 06/21/2022
-
-