• 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 
 3 
 4 
 > 
 
34 records meeting your search criteria returned- Product Code: KNT Product Problem: Material Deformation Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN CONNECT SET 07/20/2018
COVIDIEN LLC KENDALL ENTRIFLEX 07/06/2018
C.R. BARD, INC. (COVINGTON) -1018233 BARD® DIGNISHIELD® STOOL MANAGEMENT SYST 05/03/2018
COOK INC ULTRATHANE WILLS-OGLESBY PERCUTANEOUS GA 12/07/2017
APPLIED MEDICAL TECHNOLOGY, INC. AMT G-JET 07/09/2016
CONVATEC INC. FLEXI SEAL SIGNAL (FMS) SYSTEM WITH ZEOL 06/30/2016
CONVATEC INC. FLEXI SEAL SIGNAL (FMS) SYSTEM WITH ZEOL 06/30/2016
CORPAK MEDSYSTEMS CORFLO PEG KIT 16FR 05/11/2016
CONVATEC INC. FLEXI SEAL SIGNAL (FMS) 03/25/2016
CONVATEC, INC. FLEXI-SEAL ® SIGNAL® FMS® 03/04/2016
-
-