• 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
 

 
 
 1 
 2 
 > 
 
20 records meeting your search criteria returned- Product Code: LYJ Product Problem: Communication or Transmission Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CYBERONICS STIMULATOR, AUTONOMIC NERVE, IMPLANTED F 08/12/2023
LIVANOVA USA, INC. PULSE GEN MODEL 106 02/05/2021
LIVANOVA USA, INC. PULSE GEN MODEL 102 01/15/2021
LIVANOVA USA, INC. PULSE GEN MODEL 1000 01/15/2021
LIVANOVA USA, INC. PULSE GEN MODEL 103 09/04/2020
LIVANOVA USA, INC. PULSE GEN MODEL 1000 08/21/2020
LIVANOVA USA, INC. PULSE GEN MODEL 1000 06/25/2020
LIVANOVA USA, INC. PROGRAMMING SOFTWARE 06/11/2020
CYBERONICS - HOUSTON PULSE GEN MODEL 106 03/06/2020
LIVANOVA USA, INC. PULSE GEN MODEL 1000 02/07/2020
-
-