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COSMO ROBOTICS CO., Ltd.

South Korea KR-MF-000041561 Last updated 31 May 2026

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Devices
2
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue2

Authorised representatives

What COSMO ROBOTICS CO., Ltd. makes

Cosmo Robotics Co., Ltd. manufactures exoskeleton assist devices, including the ExoAtletⓇ-II for mobility support and the Bambini Teens exoskeleton designed for pediatric and adolescent users.

These devices are classified as Class IIa under EU regulations and are registered in the eudamed database. The company is based in South Korea.

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

Frequently asked questions

What types of medical devices does Cosmo Robotics Co., Ltd. manufacture?

Cosmo Robotics Co., Ltd. specializes in exoskeleton assist devices. Their portfolio includes the ExoAtletⓇ-II, which aids mobility support for adult users, and the Bambini Teens exoskeleton, specifically designed for pediatric and adolescent patients. These devices are intended to enhance movement and independence for their respective user groups.

Where is Cosmo Robotics Co., Ltd. based?

Cosmo Robotics Co., Ltd. is headquartered in South Korea. The company’s location in South Korea influences its regulatory and manufacturing operations, though its devices may be distributed globally depending on market authorization.

In which regulatory databases are Cosmo Robotics Co., Ltd.’s devices listed?

Cosmo Robotics Co., Ltd.’s devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This listing is required for devices placed on the EU market, ensuring transparency and traceability under EU regulations.

How are Cosmo Robotics Co., Ltd.’s devices classified under EU regulations?

Cosmo Robotics Co., Ltd.’s devices, including the ExoAtletⓇ-II and Bambini Teens exoskeletons, fall under Class IIa classification in the EU. This classification is determined based on factors like the device’s intended purpose, risk level, and interaction with the body. Class IIa devices require conformity assessment procedures such as a Notified Body review to ensure safety and performance before market authorization.

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

Information

Country
South Korea
Address
20, Digital-ro 31-gil, Seoul, South Korea
PRRC contact
Youngsub Shin
EUDAMED SRN
KR-MF-000041561
DUNS number
694799633