Transparency Registry · applicant
Disior, Ltd.: 4 FDA AI clearances
Every 510(k) clearance held by Disior, Ltd. under the AI-associated product codes this registry tracks, from openFDA public records, refreshed weekly. Facts only; listing is not evaluation.
| Device | Decision date | Category |
|---|---|---|
| SMART PCFD | 2025-09-29 | QIH |
| SMART Bun-Yo-Matic X-Ray | 2024-07-02 | QIH |
| SMART Bun-Yo-Matic CT | 2024-06-20 | QIH |
| Bonelogic | 2023-12-08 | QIH |
Sources linked on each entry. Coverage note: this lists clearances under tracked AI-associated codes only — the company may hold other clearances outside them. Work for Disior, Ltd.? The disclosure rows on your entries update free on submission of public links — start here.
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