Bridge TO Life, Ltd. - FDA 510(k) Cleared Devices
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.
4 devices
Not Cleared
Jan 15, 2026
VitaSmart Hypothermic Oxygenated Perfusion System
Gastroenterology & Urology
290d
Cleared
Jan 24, 2025
OrganProtex HTK Solution
Gastroenterology & Urology
266d
Cleared
Jul 01, 2021
Cannula for Organ Perfusion
Gastroenterology & Urology
238d
Cleared
Sep 24, 2019
EasiSlush
Gastroenterology & Urology
161d