Curemetrix, Inc.

FDA Regulatory Profile

Curemetrix, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 10, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K250754cmAngio® (V1.6)April 10, 2025
K232367cmAngio® V1.0October 5, 2023
K183285cmTriageMarch 8, 2019