• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
430 records meeting your search criteria returned- Product Code: GEI Patient Problem: No Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORP. PROCISE EZ COBLATOR II 09/20/2020
SMITH & NEPHEW, INC. FOOT PEDAL 09/18/2020
SMITH & NEPHEW, INC. RFB VULCAN GENERATOR CE MARK 09/18/2020
ARTHROCARE CORP. EVAC 70 XTRA HP COBLATOR II 09/17/2020
COVIDIEN MFG DC BOULDER LIGASURE 09/17/2020
ARTHROCARE CORP. WEREWOLF FLOW 50 COBLATION WAND 09/17/2020
ARTHROCARE CORP. PROCISE EZ VIEW COBLATOR II 09/16/2020
ARTHROCARE CORP. PROCISE EZ VIEW COBLATOR II 09/16/2020
ARTHROCARE CORP. RF12000 Q2 SRVC CONTROLLER-ONLY PACKAGE 09/16/2020
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 09/15/2020
-
-