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Curemetrix, Inc.

FDA Regulatory Profile

Summary

Total Recalls: 0
510(k) Clearances: 3
Inspections: 1
Compliance Actions: 0

Recent 510(k) Clearances

K-Number	Device	Date
K250754	cmAngio® (V1.6)	April 10, 2025
K232367	cmAngio® V1.0	October 5, 2023
K183285	cmTriage	March 8, 2019