• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: DTK Product Problem: Crack Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARGON MEDIAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 04/13/2024
COOK MEDICAL LLC COOK CELECT PLATINUM VENA CAVA FILTER SE 02/16/2022
CARDINAL HEALTH MEXICO OPTEASE RETRIEVABLE VENA CAVA FILTER 06/17/2021
COOK INC GUNTHER TULIP VENA CAVA FILTER RETRIEVAL 05/04/2021
CORDIS CASHEL 10FR OPTEASE RETRIEVAL CATH. 06/10/2019
CORDIS CASHEL 10FR OPTEASE RETRIEVAL CATH. 06/10/2019
CORDIS CORPORATION CATH ST 5F MP A2 (I) 125CM 2SH 01/02/2019
COOK INC GUNTHER TULIP VENA CAVA FILTER RETRIEVAL 09/18/2017
COOK INC UNKNOWN 07/18/2017
COOK INCORPORATED BIRD'S NEST VENA CAVA FILTER 06/06/2017
-
-