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

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
 

 
 
5 records meeting your search criteria returned- Product Code: KOX Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
Unknown Manufacturer TAPE ++ ADHESIVE REMOVER 04/13/2022
MUELLER SPORTS MEDICINE, INC. MUELLER BLUE KINESIOLOGY TAPE PRE-CUT ST 06/13/2019
SMITH & NEPHEW MEDICAL LTD. REMOVE WIPES 06/06/2017
SMITH & NEPHEW, INC. UNISOLVE WIPES 06/30/2015
SMITH & NEPHEW, INC. REMOVE 8OZ WIPES 04/28/2015
-
-