• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: FAE Product Problem: Appropriate Term/Code Not Available Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COLOPLAST A/S GENESIS MALLEABLE 03/11/2022
COLOPLAST A/S GENESIS MALLEABLE 01/24/2022
COLOPLAST A/S GENESIS MALLEABLE 12/21/2021
COLOPLAST A/S GENESIS MALLEABLE 12/17/2021
COLOPLAST A/S GENESIS MALLEABLE 11/08/2021
COLOPLAST A/S ALPHA I 09/13/2021
COLOPLAST A/S GENESIS MALLEABLE 09/09/2021
COLOPLAST A/S GENESIS MALLEABLE 08/23/2021
COLOPLAST A/S GENESIS MALLEABLE 06/07/2021
COLOPLAST A/S GENESIS MALLEABLE 02/18/2021
-
-