• 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: HNQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 01/16/2020
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 04/18/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 03/26/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 03/26/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 02/07/2019
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 11/15/2018
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 09/05/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 06/05/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 01/23/2018
IANTECH, INC. LOW ENERGY ENDOCAPSULAR PHACO (LEEP) DEV 12/19/2017
-
-