Medical Device Manufacturer · US , Columbia , SC

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

4 submissions · 3 cleared · Since 2019
4
Total
3
Cleared
1
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.

510(k) submissions have been managed by Wood Burditt Group as regulatory consultant.

FDA 510(k) Regulatory Record - Bridge TO Life, Ltd.
4 devices
1-4 of 4
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