Lightsense Technologies, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lightsense Technologies, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lightsense Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Lightsense Technologies, Ltd.
1 devices