• 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: Device Damaged by Another Device Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
KARL STORZ SE & CO. KG VIDEO URETERO-RENOSCOPE FLEX-XC1 10/30/2023
KARL STORZ SE & CO. KG VIDEO URETERO-RENOSCOPE FLEX-XC1 10/30/2023
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 04/25/2022
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO VIDEOSCOPE 12/04/2020
OLYMPUS MEDICAL SYSTEMS CORPORATION S CYRUS ACMI FLEXIBLE URETEROSCOPE 04/09/2020
KARL STORZ ENDOVISION VIDEO-URETERO-RENOSCOPE FLEX XC 12/11/2018
BOSTON SCIENTIFIC - SPENCER LITHOVUE SINGLE-USE DIGITAL FLEXIBLE URE 10/21/2016
OLYMPUS MEDICAL SYSTEMS CORPORATION URETERO-RENO VIDEOSCOPE 07/28/2015
OLYMPUS MEDICAL SYSTEMS CORPORATION URETERO-RENO VIDEOSCOPE 07/16/2015
-
-