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Kico Knee Innovation Company Pty Ltd

Australia·AU-MF-000011477

Last updated September 18, 2026

About

360 Med Care combines people, knowledge and technology to optimise the episode of care for patients undergoing joint replacement surgery.

From the manufacturer's own website. Source

What Kico Knee Innovation Company Pty Ltd makes

Kico Knee Innovation Company Pty Ltd manufactures orthopaedic surgical instruments and modular knee, hip, and shoulder replacement systems. Their product line includes precision guides, mounts, adapters, trays, and accessories designed for joint arthroplasty procedures, such as the 360CAS Knee and ARVIS Shoulder systems. The company also produces reusable and disposable components like the Flex Jack and Belt Pack for intraoperative use.

The company’s devices are classified under EU regulations as Class I, Class II, and Class IIa, with listings in the EUDAMED database and FDA’s 510(k) registry. Their portfolio is regulated under Australian and international medical device frameworks, ensuring compliance with relevant standards for surgical instruments and joint prosthetics. The manufacturer operates from Australia and adheres to regulatory requirements for these device categories.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Kico Knee Innovation Company Pty Ltd make?

Where is Kico Knee Innovation Company Pty Ltd based?

Kico Knee Innovation Company Pty Ltd operates from Australia, as indicated by the country code AU in the provided data. The company’s manufacturing and regulatory activities are tied to its Australian base, which supports its compliance with local and international medical device frameworks.

Which regulatory registries list devices from Kico Knee Innovation Company Pty Ltd?

Devices from Kico Knee Innovation Company Pty Ltd are listed in the EUDAMED database and the FDA’s 510(k) registry. These listings reflect the company’s compliance with European Union and United States medical device regulations for the products it manufactures.

How are the devices made by Kico Knee Innovation Company Pty Ltd classified?

The devices manufactured by Kico Knee Innovation Company Pty Ltd are classified under EU regulations as Class I, Class II, and Class IIa. This classification reflects the risk level associated with the surgical instruments and joint replacement systems they produce, such as guides, mounts, adapters, and modular prosthetics used in arthroplasty procedures.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: Australia
Address: 25, Frenchs Forest Rd E, Frenchs Forest, Australia
Website: 360med.care/
LinkedIn: linkedin.com/company/360medcare
Facebook: —
Email: [email protected]
Phone: —
PRRC Contact: —
EUDAMED SRN: AU-MF-000011477
FDA FEI Number: —
DUNS Number: —

Catalogue (36)

Device	Model / Reference	Registries	Class	Status
[ARVIS - Instruments] Mounts and Adapters	IN-16200	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Flex Jack	IN-21000	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Precision Adjustable Distal Guide	IN-19100	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-15800	EUDAMEDFDA UDI	Class I	Active
360CAS Knee	K242009	FDA 510(k)	Class II	Active
ARVIS® Shoulder	K243950	FDA 510(k)	Class II	Active
[ARVIS - Instruments] Mounts and Adapters	IN-20400	EUDAMEDFDA UDI	Class I	Active
[ARVIS] Hip and Knee	IN-14700	EUDAMEDFDA UDI	Class IIa	Active
[ARVIS] Belt Pack	IN-12500	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Instrument Tray	IN-20000	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-18900	EUDAMEDFDA UDI	Class I	Active
[ARVIS] Eyepiece Assembly	IN-12400	EUDAMEDFDA UDI	Class I	Active
[ARVIS] Headband	IN-17100	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Hex Driver	IN-10800	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-19900	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-15700	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-15900	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Tracker A, B, C	IN-16100	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Instrument Tray	IN-17300	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Instrument Tray	IN-11000	EUDAMEDFDA UDI	Class I	Active
Arvis	IN-14200	EUDAMEDFDA UDI	Class I	Active
Arvis	IN-50000	EUDAMEDFDA UDI	Class IIa	Active
[ARVIS - Instruments] Tracker A, B, C	IN-16400	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Registration Stylus, Hip and Knee	IN-18600	EUDAMEDFDA UDI	Class I	Active
[ARVIS] T7 Adapter Kit	IN-21700	EUDAMEDFDA UDI	Class I	Active
[ARVIS] Flyte Mounting Kit	IN-17500	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-16300	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-10500	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Femoral Cutting Block	IN-15600	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Tracker A, B, C	IN-10600	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-20100	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-10200	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-20200	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Mounts and Adapters	IN-20300	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Instrument Tray	IN-17200	EUDAMEDFDA UDI	Class I	Active
[ARVIS - Instruments] Tracker D	IN-10400	EUDAMEDFDA UDI	Class I	Active

Related Companies

Authorised Representatives

MedEnvoy Global BV NL

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

Kico Knee Innovation Company Pty Limited US