Ibex Galen Prostate

🟢Active

AI-powered pathology software from Ibex Medical Analytics that assists pathologists in reviewing prostate biopsy slides, detecting and grading cancer, and reporting diagnostic findings in digital pathology workflows.

Why Abandoned

Ibex continues to list Galen Prostate within its pathology platform, and the FDA granted the product Breakthrough Device Designation in 2023. Public evidence supports ongoing commercial availability, though market access varies by jurisdiction.

🩺 Health Signals

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📅 Timeline

2016-01-01

Ibex Medical Analytics founded

2021-03-09

Ibex raises $38 million Series B

2023-06-14

FDA grants Breakthrough Device Designation

2024-03-19

Ibex raises $55 million Series C

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Frequently Asked Questions

What is Ibex Galen Prostate?

Ibex Galen Prostate is AI-based clinical decision-support software for digital pathology. It analyzes digitized prostate biopsy slides to help pathologists identify cancer, grade findings, and produce diagnostic reports.

How does Ibex Galen Prostate help detect prostate cancer?

The software applies computational pathology models to whole-slide images from prostate biopsies. It highlights suspicious tissue and supplies case-level diagnostic information for review by a qualified pathologist; it is intended to support, not replace, professional judgment.

Is Ibex Galen Prostate FDA approved?

Ibex announced in June 2023 that the FDA granted Galen Prostate Breakthrough Device Designation. That designation is not the same as FDA marketing clearance or approval, and users should verify the latest regulatory status and authorized use directly with Ibex and relevant regulators.

Who makes Ibex Galen Prostate?

The product is developed by Ibex Medical Analytics, a computational pathology company founded by Joseph Mossel and Chaim Linhart in 2016.

Is Ibex Galen Prostate still available?

It appears active: Ibex continues to maintain a product page and describes Galen as part of its current pathology platform. Availability, integrations, and permitted clinical use depend on the country and applicable regulatory authorization.