# Curemetrix, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 4 (2019–2026): 4 510(k) clearances
- Product codes: QIH (3), QFM (1)
- 510(k) review time since 2016: median 80 days, against 140 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Viz.Al, Inc.: 1 (https://510kreport.com/company/viz-al)

## Firms that cite its devices most
- Zebra Medical Vision, Ltd.: 3 (https://510kreport.com/company/zebra-medical-vision)
- DeepHealth, Inc.: 2 (https://510kreport.com/company/deephealth)

## Its most-cited devices
- K183285: cmTriage (2019), cited by 4
- K250754: cmAngio® (V1.6) (2025), cited by 1

## Recent decisions
- K260980: cmAngio® V2.0 (Jul 30, 2026)
- K250754: cmAngio® (V1.6) (Apr 10, 2025)
- K232367: cmAngio® V1.0 (Oct 5, 2023)
- K183285: cmTriage (Mar 8, 2019)

Source page: https://510kreport.com/company/curemetrix