Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
344 records meeting your search criteria returned- Product Code: GEI Product Problem: No Apparent Adverse Event Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN LP - SUPERDIMENSION INC EMPRINT 02/20/2023
ARTHROCARE CORPORATION FA QUANTUM 2 CONTROLLER 02/10/2023
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 CURVED 37CM SHAFT 02/02/2023
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 01/26/2023
ARTHROCARE CORPORATION EVAC 70 XTRA HP COBLATOR II 01/19/2023
ARTHROCARE CORPORATION WEREWOLF FLOW 90 COBLATION WAND 01/11/2023
COVIDIEN MFG DC BOULDER FORCETRIAD 12/26/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
-
-