Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Bridge to Life Ltd with 6 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jan 15, 2026: VitaSmart Hypothermic Oxygenated Perfusion System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 15, 2026 | VitaSmart Hypothermic Oxygenated Perfusion SystemDEN250009 · SGY | 510(k) clearances |
| Jun 17, 2025 | EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250)K243618 · KDN | 510(k) clearances |
| Jun 12, 2025 | Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF Class II · The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits be | Device recalls |
| Mar 31, 2025 | Belzer UW® Cold Storage Solution (BTLBUW-001)K243384 · KDN | 510(k) clearances |
| Mar 26, 2025 | Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)K243840 · KDN | 510(k) clearances |
| Jan 24, 2025 | OrganProtex HTK SolutionK241239 · KDL | 510(k) clearances |
| Jul 1, 2021 | Cannula for Organ PerfusionK203262 · KDN | 510(k) clearances |
| Sep 24, 2019 | EasiSlushK191006 · KDN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
