Deski is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Deski - FDA 510(k) Cleared Devices
Recent clearances: HeartFocus, HeartFocus (V.1.1.1)
2
Total
2
Cleared
0
Denied
Deski has 2 FDA 510(k) cleared medical devices. Based in Bordeaux, FR.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Deski Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Deski
2 devices