Lanterna Medical Technologies is one of 19051 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lanterna Medical Technologies - FDA 510(k) Cleared Devices
Recent clearances: Santis Pedicle Screw System, SANTIS PEDICLE SCREW SYSTEM
2
Total
2
Cleared
0
Denied
Lanterna Medical Technologies has 2 FDA 510(k) cleared medical devices. Based in Apple Valley, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Lanterna Medical Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Silver Pine Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Lanterna Medical Technologies
2 devices