Moon Surgical is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Moon Surgical - FDA 510(k) Cleared Devices
Recent clearances: Maestro System (REF100), Maestro System (REF100), Maestro System (REF100)
4
Total
4
Cleared
0
Denied
Moon Surgical has 4 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Jun 2025. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Moon Surgical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Daniel & Daniel Consulting as regulatory consultant. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Moon Surgical
4 devices