• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: LKK Product Problem: Break Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CODMAN & SHURTLEFF CODMAN 3000 05/21/2021
MEDTRONIC, INC. BACLOFEN CATHETER 06/05/2020
MEDTRONIC NEUROMODULATION SYNCHROMED II CATHETER 09/12/2019
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 08/03/2018
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 08/02/2018
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 08/01/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 07/26/2018
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 07/13/2018
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 07/12/2018
MEDTRONIC NEUROMODULATION UNKNOWN 07/12/2018
-
-