Kico Knee Innovation Company Pty Limited is one of 142 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Kico Knee Innovation Company Pty Limited - FDA 510(k) Cleared Devices
Recent clearances: ARVIS Surgical Navigation System, 360CAS, 360CAS
4
Total
4
Cleared
0
Denied
Kico Knee Innovation Company Pty Limited has 4 FDA 510(k) cleared medical devices. Based in Pymble, AU.
Latest FDA clearance: Mar 2025. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kico Knee Innovation Company Pty Limited Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Softwarecpr and Stefanie Michele Auf Der Mauer Asmuss.
FDA 510(k) Regulatory Record - Kico Knee Innovation Company Pty Limited
4 devices