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Odc Ophthalmic Development Co. AG

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Devices
1

What Odc Ophthalmic Development Co. AG makes

Odc Ophthalmic Development Co. AG manufactures SMARTLENS, a type of intraocular lens designed for cataract surgery and refractive correction to improve vision clarity.

The company’s portfolio is regulated under FDA’s Class II device classification, with SMARTLENS authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. 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

  • Smartlens Ref K002510

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

Frequently asked questions

How many devices does Odc Ophthalmic Development Co. AG have in the registry?

The registry currently lists 1 device for Odc Ophthalmic Development Co. AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Odc Ophthalmic Development Co. AG's devices?

Among its 1 most recently registered device, Odc Ophthalmic Development Co. AG has devices listed in FDA 510(k) (1 device).

What risk classes do Odc Ophthalmic Development Co. AG's devices fall under?

Among its 1 most recently registered device, the classes recorded for Odc Ophthalmic Development Co. AG's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Odc Ophthalmic Development Co. AG in the registry?

The most recently registered devices listed for Odc Ophthalmic Development Co. AG include SMARTLENS.

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