• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
75 records meeting your search criteria returned- Product Code: IQI Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BREG, INC. BREG POST-OP SHOE 09/09/2015
BREG, INC. BREG POST-OP SHOE 06/16/2015
DEROYAL INDUSTRIES, INC DEROYAL 04/24/2015
BREG, INC. BREG POST-OP SHOE 04/16/2015
BREG, INC. BREG POST-OP SHOE 02/16/2015
BREG, INC. BREG POST-OP SHOE 12/22/2014
BREG, INC. BREG POST-OP SHOE 11/14/2014
BREG, INC. BREG POST-OP SHOE 10/10/2014
BREG, INC. BREG POST-OP SHOE 09/05/2014
BREG, INC BREG POST-OP SHOE 06/06/2014
-
-