• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
42 records meeting your search criteria returned- Product Code: FDI 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 SENSATION SHORT THROW 10/13/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 09/19/2023
BOSTON SCIENTIFIC CORPORATION CAPTIFLEX 08/16/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/30/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/30/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/30/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/30/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/30/2023
BOSTON SCIENTIFIC CORPORATION ULTRATOME XL 03/03/2022
BOSTON SCIENTIFIC CORPORATION ULTRATOME XL 10/08/2021
-
-