Kico Knee Innovation Company Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Kico Knee Innovation Company Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ARVIS® Shoulder, 360CAS Knee
2
Total
2
Cleared
0
Denied
Kico Knee Innovation Company Pty, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Frenchs Forest, AU.
Latest FDA clearance: Jan 2025. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kico Knee Innovation Company Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Stefanie Michele Auf Der Mauer Asmuss as regulatory consultant.
FDA 510(k) Regulatory Record - Kico Knee Innovation Company Pty, Ltd.
2 devices