Tempus AI (TEM) is a publicly traded Imaging & Diagnostics AI company founded in 2015 and based in Chicago, United States.
No dated funding rounds on file. This company is privately held and may be raising or operating on undisclosed capital.
Tempus AI reported Q2 2026 (quarter ended June 30, 2026) total revenue of $382.5 million, up 22% year-over-year from $314.6 million. Diagnostics revenue was $289.3 million (up 20%), and Data and Applications revenue was $93.2 million (up 28%). GAAP gross profit rose 26% to $246.5 million. GAAP net income was $5.6 million (diluted EPS $0.03), compared with a net loss of $42.8 million in Q2 2025; the release notes this figure included $98.5 million in unrealized gains on marketable securities and $55.6 million of stock compensation and related payroll taxes. GAAP loss from operations was $75.9 million. Adjusted EBITDA was $8.0 million, compared with ($5.6 million) a year earlier. Operationally, Oncology volume grew 31% and MRD volume reached 9,000 tests (from 6,500 in the prior quarter, as stated in the release). Data Licensing (Insights) revenue rose 36%, and the company signed about $200 million in new Data and Applications licenses. The FDA approved the tumor-only xT CDx assay, and the company agreed to acquire Personalis for $16.25 per share (about $1.5 billion enterprise value), expected to close in late Q4 2026 or early 2027. Full-year 2026 revenue guidance was raised to $1.595–$1.605 billion, and Adjusted EBITDA guidance of about $65 million was reaffirmed; guidance excludes the Personalis transaction.
FY2026 revenue $1.595–$1.605 billion (raised); FY2026 Adjusted EBITDA ~$65 million (reaffirmed)
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Tempus One is a generative AI assistant built for clinicians, researchers, and life-sciences teams that lets users query a large de-identified clinical and molecular data set in natural language. It surfaces patient-level insights, summarizes oncology records, and helps identify candidate clinical trials. Its differentiator is that it runs on Tempus's proprietary multimodal data library rather than general-purpose public text alone, which helps answers stay tied to real patient outcomes.
xT CDx is Tempus's comprehensive genomic profiling test for solid tumors, combining DNA and RNA sequencing to identify actionable biomarkers that guide targeted therapy selection. It is designed for oncologists and pathology labs that need a single assay covering a broad panel of cancer genes. The test is FDA-approved as a companion diagnostic, which lets it support treatment decisions on-label rather than as a research-only readout.
Paige is the pathology AI business Tempus acquired, which develops software that analyzes digitized tissue slides to support cancer diagnosis. Its tools flag suspicious regions and assist pathologists with case review, aiming to improve accuracy and throughput in anatomic pathology labs. Paige's products are built on large pathology image datasets and are offered as FDA-authorized clinical software, distinguishing them from research-only computer vision tools.