Intelesens Limited is one of 18533 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intelesens Limited - FDA 510(k) Cleared Devices
Recent clearances: zensor system, V-PATCH SYSTEM, VITALSENS, AINGEAL, V-POD
3
Total
3
Cleared
0
Denied
Intelesens Limited has 3 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Historical record: 3 cleared submissions from 2011 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intelesens Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Promedic, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Intelesens Limited
3 devices