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
 

 
 
 1 
 2 
 > 
 
13 records meeting your search criteria returned- Product Code: HQF Product Problem: Device Inoperable Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LIO, LASER INDIRECT OPHTHALMOS 04/20/2018
D.O.R.C INTERNATIONAL EVA, COMBINED MACHINE INCLUDING LASER (D 01/24/2018
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 10/16/2017
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 05/19/2017
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 12/16/2016
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 10/11/2016
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 06/02/2016
ALCON ILLUMINATED FLEXIBLE 01/12/2016
IRIDEX CORPORATION OCULIGHT GLX 10/16/2015
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY PUREPOINT LASER 07/09/2015
-
-