• 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 
 > 
 
58 records meeting your search criteria returned- Product Code: MJO Product Problem: Expulsion Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT M"STANDARD", UNKNOWN SIZE 11/14/2022
CENTINEL SPINE PRODISC C US IMPLANT MEDIUM 5MM 11/02/2022
CENTINEL SPINE, LLC. PRODISC L SUPERIOR PLATE, SIZE MEDIUM, 1 03/17/2022
CENTINEL SPINE, LLC. PRODISC L PE-INLAY W/ X-RAY MARKER, STER 03/17/2022
CENTINEL SPINE, LLC. INFERIOR END PLATE MEDIUM 0-STERILE 03/17/2022
CENTINEL SPINE, LLC. PRODISC L SUPERIOR PLATE, SIZE MEDIUM, 6 03/17/2022
CENTINEL SPINE, LLC. PRODISC L PE-INLAY W/ X-RAY MARKER, STER 03/17/2022
CENTINEL SPINE, LLC. INFERIOR END PLATE MEDIUM 0-STERILE 03/17/2022
CENTINEL SPINE, LLC. PRODISC L PE-INLAY W/ X-RAY MARKER, STER 11/16/2021
CENTINEL SPINE, LLC. PRODISC L INFERIOR END PLATE LARGE 0-STE 11/16/2021
-
-