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 
 > 
 
36 records meeting your search criteria returned- Product Code: MJO Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CENTINEL SPINE, LLC SUPERIOR END PLATE MEDIUM 3-STERILE 03/24/2022
CENTINEL SPINE, LLC INFERIOR END PLATE MEDIUM 8-STERILE 03/24/2022
CENTINEL SPINE, LLC PRODISC L PE-INLAY W/ X-RAY MARKER, STER 03/24/2022
CENTINEL SPINE, LLC. PRODISC C US IMPLANT MEDIUM 6MM 11/30/2021
CENTINEL SPINE, LLC. PRODISC C US IMPLANT MEDIUM 6MM 11/30/2021
LDR MÉDICAL IMPLANT MOBIC M ST 15X17 H7 US 09/07/2021
LDR MÉDICAL IMPLANT MOBIC M ST 13X15 H6 US 09/07/2021
LDR MÉDICAL IMPLANT MOBIC M ST 15X17 H6 US 08/23/2021
CENTINEL SPINE, LLC. PRODISC C US TOTAL DISC REPLACEMENT 07/29/2021
CENTINEL SPINE, LLC. PRODISC C TOTAL DISC REPLACEMENT 07/15/2020
-
-