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Amore Mio, Inc.

Country not established

Devices
1

What Amore Mio, Inc. makes

Amore Mio, Inc. manufactures spectacle frames, which are designed for use in eyeglasses and provide structural support for lenses.

These products fall under Class I medical devices and are listed in the FDA’s 510(k) registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Spectacle Frames Ref K941523

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

Frequently asked questions

How many devices does Amore Mio, Inc. have in the registry?

The registry currently lists 1 device for Amore Mio, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Amore Mio, Inc.'s devices?

Among its 1 most recently registered device, Amore Mio, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Amore Mio, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Amore Mio, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Amore Mio, Inc. in the registry?

The most recently registered devices listed for Amore Mio, Inc. include SPECTACLE FRAMES.

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