Transparency Registry · applicant
Curemetrix, Inc.: 4 FDA AI clearances
Every 510(k) clearance held by Curemetrix, 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 |
|---|---|---|
| cmAngio® V2.0 | 2026-07-30 | QIH |
| cmAngio® (V1.6) | 2025-04-10 | QIH |
| cmAngio® V1.0 | 2023-10-05 | QIH |
| cmTriage | 2019-03-08 | QFM |
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 Curemetrix, Inc.? The disclosure rows on your entries update free on submission of public links — start here.
Link to this page. Many companies reference
their registry listing from press pages and footers — it is a neutral,
weekly-verified public record. Copy either snippet:
Text link:
Badge: