Chirurgie Innovation is one of 281 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Chirurgie Innovation - FDA 510(k) Cleared Devices
Recent clearances: Plasma Edge resection and vaporization electrodes, Plasma Edge working elements, Adaptor Plasma Edge, Plasma Edge System
2
Total
2
Cleared
0
Denied
Chirurgie Innovation has 2 FDA 510(k) cleared medical devices. Based in Massy, FR.
Last cleared in 2022. Active since 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Chirurgie Innovation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Chirurgie Innovation
2 devices