Medical Device Manufacturer · US , Columbia , SC

Bridge TO Life, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2019

Total

Cleared

Denied

Bridge TO Life, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Columbia, US.

Latest FDA clearance: Jan 2025. Active since 2019. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Bridge TO Life, Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by The Wood Burditt Group and Wood Burditt Group.

Bridge TO Life, Ltd. 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 - Bridge TO Life, Ltd.

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 27, 2026