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
 

 
 
 1 
 2 
 3 
 4 
 > 
 
38 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Impaired Healing Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA USA, INC. PULSE GEN MODEL 1000 04/29/2024
LIVANOVA USA, INC. PULSE GEN MODEL 1000-D 03/15/2024
LIVANOVA USA, INC. PULSE GEN UNKNOWN 01/16/2024
LIVANOVA USA, INC. PULSE GEN MODEL 1000 12/01/2023
CYBERONICS - HOUSTON LEAD MODEL 300 11/14/2023
LIVANOVA USA, INC. LEAD MODEL 304 11/03/2023
CYBERONICS - HOUSTON LEAD MODEL 304 05/02/2023
LIVANOVA USA, INC. PULSE GEN MODEL 106 04/14/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 105 03/23/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 106 02/16/2023
-
-