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Kiro Robotics S.L.

SpainFDA applicant, unverified

Devices
1

What Kiro Robotics S.L. makes

Kiro Robotics S.L. manufactures the KIRO Set, a robotic system designed for surgical applications, including minimally invasive procedures.

The KIRO Set is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • KIRO Set Ref K152441

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Kiro Robotics S.L. have in the registry?

The registry currently lists 1 device for Kiro Robotics S.L.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kiro Robotics S.L.'s devices?

Among its 1 most recently registered device, Kiro Robotics S.L. has devices listed in FDA 510(k) (1 device).

What risk classes do Kiro Robotics S.L.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Kiro Robotics S.L.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kiro Robotics S.L. in the registry?

The most recently registered devices listed for Kiro Robotics S.L. include KIRO Set.

Generated automatically from registry data and not verified by a human reviewer.