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Buffard-La-Doye

Country not established

Devices
1

What Buffard-La-Doye makes

Buffard-La-Doye manufactures spectacle frames designed for corrective and fashion eyewear. These products include standard and customizable frame styles intended for general optical use.

The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The products are listed in the FDA’s 510(k) database. The manufacturer 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

  • Spectacle Frames Ref K943326

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Buffard-La-Doye have in the registry?

The registry currently lists 1 device for Buffard-La-Doye. Devices recorded under merged duplicate company entries are counted once.

Which registries list Buffard-La-Doye's devices?

Among its 1 most recently registered device, Buffard-La-Doye has devices listed in FDA 510(k) (1 device).

What risk classes do Buffard-La-Doye's devices fall under?

Among its 1 most recently registered device, the classes recorded for Buffard-La-Doye's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Buffard-La-Doye in the registry?

The most recently registered devices listed for Buffard-La-Doye include SPECTACLE FRAMES.

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