Transparency Registry · applicant
Viz. Ai, Inc.: 9 FDA AI clearances
Every 510(k) clearance held by Viz. Ai, 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 |
|---|---|---|
| Viz Subdural+, Viz SUBDURAL PLUS | 2025-06-10 | QIH |
| Viz HDS, Viz Volume Plus, Viz ICH+ | 2024-02-05 | QIH |
| Viz AAA | 2023-03-17 | QFM |
| Viz LVO ContaCT | 2022-10-21 | QAS |
| Viz RV/LV | 2022-08-29 | QIH |
| Viz SDH | 2022-07-25 | QAS |
| Viz ANEURYSM, Viz ANX | 2022-02-18 | QFM |
| Viz ICH | 2021-03-23 | QAS |
| Viz ICH | 2020-03-18 | QAS |
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 Viz. Ai, Inc.? The disclosure rows on your entries update free on submission of public links — start here.
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