• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
94 records meeting your search criteria returned- Product Code: EHD 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
GENDER DENTAL SYSTEMS 765DC 12/10/2014
ARIBEX, INC. NOMAD PRO 11/03/2014
GENDEX GENDEX EXPERT DC 10/31/2014
MIDMARK CORP. PROGENY PREVA 10/28/2014
GENDEX DENTAL SYSTEMS 765DC 10/16/2014
ARIBEX, INC. NOMAD PRO 10/14/2014
MIDMARK CORP PROGENCY JB-70 09/18/2014
GENDEX CORP. GENDEX GX-770 09/15/2014
GENDEX CORP. GENDEX GX-770 09/15/2014
MIDMARK CORPORATION VETPRO 09/04/2014
-
-