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 
 
 
11 records meeting your search criteria returned- Product Code: HQE Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 10/19/2023
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 08/16/2023
D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTE EVA NEXUS¿ POSTERIOR 25G TDC PACK 06/19/2023
ALCON RESEARCH, LLC - HOUSTON HYPERVIT VITRECTOMY PROBE 11/03/2021
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 04/05/2021
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 01/06/2020
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 10/11/2019
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 09/03/2019
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 06/04/2019
ALCON GRIESHABER AG BACKFLUSH HANDLE DSP 07/23/2018
-
-