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Ariel

Country not established

Devices
2

What Ariel makes

Ariel manufactures The GALASSIA System, a medical device designed for [specific clinical application, if implied by context—here omitted as not provided; adjust if additional details were given]. This system is intended for [brief functional purpose, e.g., 'diagnostic imaging,' 'patient monitoring,' or 'treatment delivery,' based on device class inference].

The GALASSIA System is regulated under the FDA’s 510(k) pathway, classifying it as a [Class I/II/III—here omitted as not specified; adjust if device class were listed]. It is listed in the U.S. under the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Af/System Ref K791192

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

  • The Galassia System Ref K791191

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

Frequently asked questions

How many devices does Ariel have in the registry?

The registry currently lists 2 devices for Ariel. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ariel's devices?

Among its 2 most recently registered devices, Ariel has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Ariel in the registry?

The most recently registered devices listed for Ariel include AF/SYSTEM and THE GALASSIA SYSTEM.

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