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Aidoc
Radiology AI company with the first FDA-cleared foundation-model triage platform (CARE, January 2026); oncology-relevant for incidental findings and workflow.
Overview
CARE foundation model cleared with 11 new indications in one workflow (mean sensitivity 97%, specificity 98% in the pivotal study); Breakthrough Device designation (June 2026) for First Read, which drafts chest radiograph reports. Not oncology-specific but sets the regulatory template for imaging foundation models.
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fronts
technologies
companies
roadmaps
ideas
AI clears the normal lung screening scans so radiologists read only the suspicious onesAI-assisted central imaging reads to cut endpoint cost and variabilityEvery routine CT scan checked by AI for early cancer signs, with a tracked follow-up pathwayNo clinical claims for imaging-derived biomarkers without phantom and standards compliance
bottlenecks
Software in use
The software of oncology →Commercial and regulated products that this organisation sells. Each card says what is behind it: a regulator's database, the literature, a public body's list, or only the company's own words. Listing is not endorsement, and a clearance is a regulatory fact, not a clinical one.
Aidoc's family of triage algorithms that push suspected findings on CT to the top of a radiologist's worklist, including incidental findings that matter in cancer care.