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
 

 
 
9 records meeting your search criteria returned- Product Code: FGB Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AURIS HEALTH, INC. MONARCH PLATFORM, UROLOGY 02/29/2024
AIZU OLYMPUS CO., LTD. URETERO-RENO VIDEOSCOPE 04/05/2023
AIZU OLYMPUS CO., LTD. URETERO-RENO FIBERSCOPE 03/20/2023
AIZU OLYMPUS CO., LTD. FORCEPS/IRRIGATION PLUG (ISOLATED TYPE) 10/19/2022
AIZU OLYMPUS CO., LTD. FORCEPS/IRRIGATION PLUG (ISOLATED TYPE) 10/19/2022
AIZU OLYMPUS CO., LTD. FORCEPS/IRRIGATION PLUG (ISOLATED TYPE) 10/19/2022
KARL STORZ ENDOVISION, INC. URETERO-RENO-FIBERSCOPE 05/09/2022
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 03/10/2021
PHILIPS FLEXVISION 02/26/2015
-
-