• 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
 

 
 
10 records meeting your search criteria returned- Product Code: DWS Patient Problem: Foreign Body In Patient Report Date From: 01/1/2009

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
ATRICURE, INC. HERCULES UNIVERSAL STABILIZER ARM 09/09/2022
SCANLAN INTERNATIONAL, INC. TUNNELER SHEATH, SMALL GREEN 06/10/2022
INTEGRA LIFESCIENCES MANSFIELD CARB-BITE COOLEY-BAUM WIRE TWIST 8 12/21/2021
CAREFUSION, INC KAYE-FREEMAN D-SEREDG SCISSR CVD 7IN 10/21/2021
GEOMED MEDIZIN-TECHNIK GMBH & CO. KG CARB-BITE MAYO-HEGAR NEEDLE HOLDER 6 09/20/2019
SCANLAN TUNNELER SHEATH AND BULLET TIP 09/05/2017
ATRICURE, INC. UNIVERSAL STABILIZER ARM, HERCULES 3 06/22/2017
W.L. GORE & ASSOCIATES GORE TUNNELER 06/16/2017
-
-