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
 

 
 
8 records meeting your search criteria returned- Product Code: DWS Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SCANLAN INTERNATIONAL SCANLAN VASCULAR TUNNELER 03/28/2024
SCANLAN INTERNATIONAL SCANLAN VASCULAR TUNNELER 03/28/2024
INTEGRA LIFESCIENCES MANSFIELD UNKNOWN JARIT 12/31/2023
INTEGRA LIFESCIENCES MANSFIELD UNKNOWN JARIT 12/31/2023
INTEGRA LIFESCIENCES MANSFIELD CARB-BITE MAYO-HEGAR NH 6 10/14/2022
SCANLAN INTERNATIONAL, INC. TUNNELER SHEATH, SMALL GREEN 06/10/2022
ATRICURE, INC. UNIVERSAL STABILIZER ARM, HERCULES 2 09/04/2020
AESCULAP AG VARADY VARIX EXTRACTOR W/CATCH 180MM 08/28/2020
-
-