Transparency Registry · applicant
Exo, Inc.: 3 FDA AI clearances
Every 510(k) clearance held by Exo, Inc. 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 |
|---|---|---|
| Strain AI (SAI001) | 2024-11-20 | QIH |
| AI Platform (AIP001) | 2023-11-17 | QIH |
| Bladder AI (AIBV01) | 2023-06-22 | 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 Exo, Inc.? The disclosure rows on your entries update free on submission of public links — start here.
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