Diabeloop is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Diabeloop - FDA 510(k) Cleared Devices
Recent clearances: DBLG2
1
Total
1
Cleared
0
Denied
Diabeloop has 1 FDA 510(k) cleared medical devices. Based in Grenoble, FR.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diabeloop Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Diabeloop
1 devices