• 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 
 > 
 
299 records meeting your search criteria returned- Product Code: GEI Product Problem: Smoking Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ENDOSCOPY-SAN JOSE PKG, CROSSFIRE 2 CONSOLE 04/24/2023
CONMED CORPORATION EXCALIBUR 04/21/2023
ARTHROCARE CORPORATION FA QUANTUM 2 CONTROLLER 04/19/2023
MEDTRONIC, INC. PS210-030S-LIGHT 04/17/2023
STRYKER ENDOSCOPY-SAN JOSE PKG, CROSSFIRE 2 CONSOLE 03/30/2023
ARTHROCARE CORPORATION FA COBLATOR II CONTROLLER (120V) 03/29/2023
INTEGRA LIFESCIENCES MANSFIELD MONO CABLE 10 FEET (3 METERS) 03/29/2023
ARTHROCARE CORPORATION WEREWOLF RF 20000 CONTROLLER 03/26/2023
ARTHROCARE CORPORATION WEREWOLF RF 20000 CONTROLLER 03/20/2023
ARTHROCARE CORPORATION PROCISE MAX COBLATOR II 03/14/2023
-
-