Lacerta Life Sciences - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lacerta Life Sciences has 1 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lacerta Life Sciences Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Lacerta Life Sciences
1 devices