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.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
1 devices