• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: HJO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
VISIA IMAGING SRL ALADDIN HW3.0 07/13/2023
VISIA IMAGING S.R.L. ALADDIN HW3.0 07/11/2023
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 03/10/2023
CARL ZEISS MEDITEC AG (JENA) IOLMASTER XP 08/12/2022
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 08/06/2021
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 07/29/2021
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 07/29/2021
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 07/29/2021
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 07/16/2021
CARL ZEISS MEDITEC AG (JENA) IOLMASTER XP 07/12/2021
-
-