X6 Innovations is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
X6 Innovations - FDA 510(k) Cleared Devices
Recent clearances: Perifit Pump, Perifit Care+, Perifit
3
Total
3
Cleared
0
Denied
X6 Innovations has 3 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Jan 2024. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by X6 Innovations Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - X6 Innovations
3 devices