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Luxottica Group SpA

Country not established FDA

Part of LUXOTTICA Group SpA

Devices
40
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Luxottica Group SpA makes

The company manufactures air-conduction hearing aids designed for use with spectacles, including the nuance audio line, which integrates auditory assistance with eyewear.

These devices fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue40

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Company details

DUNS number
436825376

FDA establishments1

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

  • LUXOTTICA Group SPA AGORDO Belluno · IT FEI 3001654059

Frequently asked questions

How many devices does LUXOTTICA GROUP SPA have in the registry?

The registry currently lists 40 devices for LUXOTTICA GROUP SPA. Devices recorded under merged duplicate company entries are counted once.

Which registries list LUXOTTICA GROUP SPA's devices?

Among its 40 most recently registered devices, LUXOTTICA GROUP SPA has devices listed in EUDAMED (3 devices) and FDA GUDID (40 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do LUXOTTICA GROUP SPA's devices fall under?

Among its 40 most recently registered devices, the classes recorded for LUXOTTICA GROUP SPA's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from LUXOTTICA GROUP SPA in the registry?

The most recently registered devices listed for LUXOTTICA GROUP SPA include nuance audio AW5001754, nuance audio AW5004756, nuance audio AW5002748 and nuance audio AW5002948.

Which FDA establishments are linked to LUXOTTICA GROUP SPA?

1 FDA establishment is linked to LUXOTTICA GROUP SPA in the registry; they are listed on the company page.

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