In 2025, 252 of the 467 510(k) clearances tagged with the FDA's radiology review committee (54.0%) were for devices on the FDA's AI-Enabled Medical Device List, by Kent Applied's count.

54.0%

of the 510(k) clearances tagged with the FDA's radiology review committee in 2025 were for devices on its AI list

In 2025, 252 of the 467 510(k) clearances tagged with the FDA's radiology review committee (54.0%) were for devices on the FDA's AI-Enabled Medical Device List, by Kent Applied's count.

Across every other review committee together, the share was 2.8%, 77 of 2,731 clearances.

Sources: FDA, Artificial Intelligence-Enabled Medical Devices (opens in a new tab), The list (CSV), content current as of September 4, 2026: Date of Final Decision, Submission Number, Panel (Lead), Primary Product Code; FDA, 510(k) releasable files (opens in a new tab), pmn96cur.txt (October 26, 2026): DATERECEIVED, DECISIONDATE, DECISION, REVIEWADVISECOMM, TYPE, COUNTRY_CODE. Verified October 2026.

KentAppliedkentapplied.com/facts/fda-ai-devices-radiology-committee-54-percent-2025

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