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Pharosystems, Inc.

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Devices
1

What Pharosystems, Inc. makes

Pharosystems, Inc. manufactures the Phako Systems VIA 2000, a device used in ophthalmic surgery for intraocular lens (IOL) implantation and cataract removal procedures.

The Phako Systems VIA 2000 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. 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

  • Phako Systems Via 2000 Ref K833642

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

Frequently asked questions

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

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

Which registries list Pharosystems, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Pharosystems, Inc. include PHAKO SYSTEMS VIA 2000.

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