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
 

 
 
7 records meeting your search criteria returned- Product Code: FCG Product Problem: Defective Device Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN LLC SHARKCORE FINE NEEDLE BIOPSY SYSTEM 22GA 03/27/2023
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 01/14/2022
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 11/30/2021
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 11/09/2021
OLYMPUS MEDICAL SYSTEMS CORP. BIOPSY NEEDLE 09/24/2021
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/04/2021
UNITED STATES ENDOSCOPY GROUP, INC CARR-LOCKE INJECTION NEEDLE 09/18/2019
-
-