NOOANCE - FDA 510(k) Cleared Devices

NOOANCE has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.

Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by NOOANCE Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Shenzhen Kaiyan Medical Equipment Co., Ltd. as regulatory consultant.