LifeLens Technologies, Inc. - FDA 510(k) Cleared Devices

LifeLens Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Warminster, US.

Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by LifeLens Technologies, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mcra, LLC as regulatory consultant.