Curemetrix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curemetrix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: cmAngio® (V1.6), cmAngio® V1.0, cmTriage
4
Total
4
Cleared
0
Denied
Curemetrix, Inc. has 4 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Latest FDA clearance: Jul 2026. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Curemetrix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Curemetrix, Inc.
4 devices