• 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 
 > 
 
123 records meeting your search criteria returned- Product Code: GEI Product Problem: Noise, Audible Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. ELECTROSURGICAL UNIT 04/27/2022
SOLTA MEDICAL, INC THERMAGE FLX (TG-3A) SYSTEM AND ACCESSOR 04/20/2022
ETHICON ENDO-SURGERY, LLC. EES GENERATOR 03/30/2022
COVIDIEN MFG DC BOULDER LIGASURE 03/23/2022
ARTHROCARE CORP. WEREWOLF RF 20000 CONTROLLER 03/02/2022
COVIDIEN MFG DC BOULDER FORCETRIAD 02/03/2022
SOLTA MEDICAL, INC THERMAGE CPT SYSTEM 01/21/2022
GYRUS ACMI, INC G400 GENERATOR, GYRUS 01/19/2022
DEPUY MITEK LLC US VAPR3 GENERATOR 11/29/2021
OLYMPUS MEDICAL SYSTEMS CORP. ELECTROSURGICAL UNIT 11/24/2021
-
-