Headquarters
New York, NYFounded
2017CEO / Founder
Leo GradyEmployees
201-500Funding
Acquired — $215MProducts
1 product listedAvg. AI Score
7.9/10Website
www.paige.aiProfile updated
Paige is a digital pathology AI company founded in 2017 in New York as a Memorial Sloan Kettering Cancer Center spinout by Thomas Fuchs and colleagues. Its AI platform supports pathologists in cancer diagnosis with FDA-cleared decision-support tools.
Paige's FullFocus slide viewer and Paige Prostate Detect were the first FDA-authorized AI applications for digital pathology in the United States. The company serves reference labs, health systems, and biopharma partners.
Paige has raised approximately $215 million, including a $100 million Series C led by Casdin Capital and Johnson & Johnson Innovation – JJDC. Leo Grady, formerly CEO of HeartFlow, joined as CEO in 2019.
Dated, source-cited figures. Estimates are marked.
All products by Paige.ai reviewed by our AI panel of experts.
Six independent reviewer personalities assessed Paige.ai's product on their own terms. They disagreed by 2.4 points — The Finance Lead was the hardest to convince, The Domain Strategist the most positive.
Averaged across 1 reviewed product in our catalog. Scores are out of 10.
Who Paige.ai competes with, and how they differ.
PathAI pairs its AI platform with pathology lab services (via its Poplar Healthcare acquisition) and focuses heavily on pharma biomarker and companion-diagnostic development, while Paige built FDA-authorized products (Paige Prostate, Paige Breast) aimed directly at clinical diagnostic use in hospital labs.
1 product reviewed on TopReviewedLunit's AI portfolio is radiology-first (Lunit INSIGHT for chest X-ray and mammography screening), with its newer Lunit SCOPE pathology line a smaller addition versus Paige's pathology-only focus and its longer track record of FDA-cleared cancer-detection products.
1 product reviewed on TopReviewedProscia sells a cloud-based digital pathology image-management and AI platform (Concentriq) to labs and pharma customers, competing with Paige on pathology workflow infrastructure rather than matching Paige's FDA-authorized diagnostic AI models.
Key milestones in Paige.ai's history, with sources.
Acquired by Tempus AI for $81.25M
Tempus AI (NASDAQ: TEM) acquired Paige for $81.25 million, paid primarily in stock, gaining almost 7 million digitized pathology slides and clinical/molecular data spanning 45 countries to accelerate its oncology foundation model.
medtechdive.comVirchow2 and Virchow2G foundation models released
Paige and Microsoft unveiled Virchow2 and Virchow2G, the second generation of their million-slide pathology foundation models, adding greater data diversity and depth for cancer detection.
paige.aiMicrosoft Research partnership to build pathology foundation model
Paige announced a collaboration with Microsoft Research to build what the companies called the world's largest image-based AI foundation model for digital pathology and oncology, later released as Virchow.
paige.aiFDA authorizes Paige Prostate -- first AI pathology product cleared
The FDA granted De Novo marketing authorization for Paige Prostate, the first AI-based software authorized to help pathologists detect prostate cancer in digitized biopsy slides; a clinical study of 16 pathologists on 527 slides showed a 7.3-point accuracy improvement.
mobihealthnews.comSeries C -- $100M initial close
Paige raised a $100 million Series C round co-led by Casdin Capital and Johnson & Johnson Innovation - JJDC; the round grew to over $125 million after a final tranche led by KKR Health Care Strategic Growth Fund closed in March 2021.
mobihealthnews.comCE Mark for Paige Prostate and Paige Breast AI
Paige received CE Marks for its AI-based prostate cancer grading/quantification and breast cancer detection software, clearing the products for use in labs and hospitals across the European Economic Area, Switzerland and the UK.
businesswire.comSeries B -- $70M
Paige raised a $70 million Series B round to advance its AI-based computational pathology products for cancer diagnosis.
aibusiness.comLeo Grady named CEO
Paige named med-tech executive Leo Grady, previously of HeartFlow, as its first CEO to lead commercialization of its AI pathology products.
wsj.comFDA grants Breakthrough Device designation
Paige's AI pathology software received FDA Breakthrough Device designation in 2019, its first US regulatory recognition ahead of the 2021 De Novo authorization for Paige Prostate.
mobihealthnews.comPublic launch to apply AI to cancer pathology
Paige.AI launched publicly, announcing its mission to bring AI-based computational pathology tools to cancer diagnosis and treatment, built on IP licensed from Memorial Sloan Kettering.
businesswire.comFounded as a Memorial Sloan Kettering spinout
Paige (originally Paige.AI) was founded in 2017 by Thomas Fuchs, Christopher Selby and David Klimstra -- chair of pathology at Memorial Sloan Kettering Cancer Center -- after MSK licensed its computational pathology intellectual property to the new company.
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