# Kico Knee Innovation Company Pty Limited

- Location (FDA's records): Frenchs Forest, AU
- FDA decisions: 6 (2017–2025): 6 510(k) clearances
- Names in FDA's records: Kico Knee Innovation Company Pty Limited (4); Kico Knee Innovation Company Pty, Ltd. (2)
- Product codes: OLO (3), SBF (2), LLZ (1)
- 510(k) review time since 2016: median 59 days, against 90 for FDA's reviews in the same codes and years (5 of 6 faster)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Insight Medical Systems, Inc.: 2 (https://510kreport.com/company/insight-medical-systems)
- Stryker Leibinger GmbH & Co KG: 1 (https://510kreport.com/company/stryker-leibinger)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Lexi Co., Ltd.: 1 (https://510kreport.com/company/lexi)

## Its most-cited devices
- K223927: 360CAS (2023), cited by 1
- K213380: 360CAS (2022), cited by 1

## Recent decisions
- K243980: ARVIS Surgical Navigation System (Mar 21, 2025)
- K243950: ARVIS® Shoulder (Jan 13, 2025)
- K242009: 360CAS Knee (Aug 8, 2024)
- K223927: 360CAS (Jan 27, 2023)
- K213380: 360CAS (Jan 11, 2022)
- K163405: 360KS Implant Positioning System (Mar 21, 2017)

Source page: https://510kreport.com/company/kico-knee-innovation