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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 5 
 6 
 > 
 
56 records meeting your search criteria returned- Product Code: LKK Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION SYNCHROMED II 04/05/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 01/13/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 01/11/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 12/13/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 12/07/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/31/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/01/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/20/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/21/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/01/2022
-
-