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

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
 

 
 
10 records meeting your search criteria returned- Product Code: FGB Product Problem: Unintended Movement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SHIRAKAWA OLYMPUS CO., LTD. URETERO-RENO VIDEOSCOPE 03/27/2023
AIZU OLYMPUS CO., LTD. URETERO-RENO VIDEOSCOPE 02/09/2023
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 12/23/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 12/05/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 12/02/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 10/21/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 10/21/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 10/01/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 09/15/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 07/18/2021
-
-