Lincotek Medical - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lincotek Medical has 2 FDA 510(k) cleared medical devices. Based in Bartlett, US.
Latest FDA clearance: Mar 2026. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Lincotek Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global as regulatory consultant.
2 devices