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Borani Intl.

Country not established

Devices
1

What Borani Intl. makes

Borani Intl. manufactures hard resin intraocular lenses, designed for cataract surgery to replace the natural lens in the eye.

These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company 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

  • Lens, Hard Resin Ref K772221

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

Frequently asked questions

How many devices does Borani Intl. have in the registry?

The registry currently lists 1 device for Borani Intl.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Borani Intl.'s devices?

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

What risk classes do Borani Intl.'s devices fall under?

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

What are the newest devices from Borani Intl. in the registry?

The most recently registered devices listed for Borani Intl. include LENS, HARD RESIN.

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