Medical Device Manufacturer · US , Fremont , CA

Lifesignals, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2020

Total

Cleared

Denied

Lifesignals, Inc. has 4 FDA 510(k) cleared medical devices. Based in Fremont, US.

Latest FDA clearance: Jul 2026. Active since 2020. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.

Lifesignals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lifesignals, Inc.

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Aug 06, 2026