Letus Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Letus Corporation has 1 FDA 510(k) cleared medical devices. Based in Happy Valley, US.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Letus Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
1 devices