• 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
 

 
 
5 records meeting your search criteria returned- Product Code: HXX Product Problem: Activation, Positioning or Separation Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH THORACIC PEDICLE PROBE 01/03/2024
SYNTHES GMBH INNER SHAFT FOR EXTRACTION SCREWDRIVER 12/22/2022
SYNTHES GMBH 3.5MM HEXAGONAL SCREWDRIVER SHAFT-6MM HX 12/19/2022
SYNTHES GMBH SYNFIX® EVOLUTION SCREWDRIVER 08/24/2021
PRECISION SPINE, INC. NEXGEN ANTERIOR CERVICAL PLATE SYSTEM 08/27/2020
-
-