Kico Knee Innovation Company Pty, Ltd.

Kico Knee Innovation Company Pty, Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 2024, most recent 2025.

Top product codes for Kico Knee Innovation Company Pty, Ltd.

OLO — Neurology1 device
SBF — Neurology1 device

Recent clearances by Kico Knee Innovation Company Pty, Ltd.

K243950 — ARVIS® ShoulderCode SBF·2025-01-13
K242009 — 360CAS KneeCode OLO·2024-08-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.