LifeLens Technologies, Inc. is one of 16099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
LifeLens Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LifeLens Physiological Monitor, LifeLens Wireless ECG Monitor
2
Total
2
Cleared
0
Denied
LifeLens Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Warminster, US.
Latest FDA clearance: Jul 2026. 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.
Regulatory submissions have been managed by Mcra, LLC and MEDIcept, Inc..
FDA 510(k) Regulatory Record - LifeLens Technologies, Inc.
2 devices