Medical Device Manufacturer · AU , Pymble

Kico Knee Innovation Company Pty Limited - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017
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.

FDA 510(k) cleared devices by Kico Knee Innovation Company Pty Limited

4 devices
1-4 of 4
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