• 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 
 3 
 4 
 5 
 > 
 
48 records meeting your search criteria returned- Product Code: HQF Product Problem: Appropriate Term/Code Not Available Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IRIDEX CORPORATION G-PROBE 02/03/2022
IRIDEX CORPORATION CUST-CYLCO-G6 01/06/2022
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY PUREPOINT LASER 12/17/2021
IRIDEX CORPORATION CUST-CYLCO-G6 10/21/2021
IRIDEX CORPORATION GLX 08/26/2021
Unknown Manufacturer PUREPOINT LASER 08/17/2021
IRIDEX CORPORATION LASER INSTRUMENT, SURGICAL, POWERED, PRO 08/02/2021
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY PUREPOINT LASER 07/20/2021
ALCON RESEARCH, LLC - IRVINE TECHNOLOGY PUREPOINT LASER 06/02/2021
ELLEX MEDICAL PTY LTD TANGO 01/18/2021
-
-