• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
309 records meeting your search criteria returned- Product Code: GEI Product Problem: Defective Device Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION REZUM 11/22/2021
GYRUS ACMI, INC PK CUTTING FORCEPS, 5MM, 33CM 11/02/2021
GYRUS ACMI, INC PK CUTTING FORCEPS, 5MM, 33CM 11/02/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO VIRTUOSAPH PLUS, WITH RADIAL 10/28/2021
ENCISION, INC. AEM MONITOR 10/28/2021
GYRUS ACMI, INC PK CUTTING FORCEPS, 5MM, 33CM 10/14/2021
MICROLINE SURGICAL, INC. MICROLINE CARDIO FORCEPS 10/13/2021
BOSTON SCIENTIFIC CORPORATION REZUM 09/29/2021
SURGICAL INNOVATIONS LIMITED LOGI RANGE 09/22/2021
BOSTON SCIENTIFIC CORPORATION LEVEEN SUPERSLIM 09/20/2021
-
-