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Unilens Corp., USA

Also registered as Unilens Corporation, USA

United StatesFDA applicant, unverified

Devices
21

What Unilens Corp., USA makes

Unilens Corp. manufactures a range of soft (hydrophilic) contact lenses, including single-vision, aspheric, bifocal, toric, and multifocal designs. Their portfolio includes lenses made from materials such as polymacon, methafilcon A, and hioxifilcon D, catering to various vision correction needs. Examples include the CVUE Advanced, Power Plus, SimulVue 38, and Axion Plus, among others.

The company’s devices are regulated under FDA classifications, including Class II, Class III, and Class U. Products are listed via 510(k) and PMA pathways, reflecting their compliance with U.S. medical device regulations. Unilens Corp. is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Unilens Corp., USA have in the registry?

The registry currently lists 21 devices for Unilens Corp., USA. Devices recorded under merged duplicate company entries are counted once.

Which registries list Unilens Corp., USA's devices?

Among its 21 most recently registered devices, Unilens Corp., USA has devices listed in FDA 510(k) (14 devices) and FDA PMA (7 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Unilens Corp., USA's devices fall under?

Among its 21 most recently registered devices, the classes recorded for Unilens Corp., USA's devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Unilens Corp., USA in the registry?

The most recently registered devices listed for Unilens Corp., USA include CVUE ADVANCED (HIOXIFILCON D) SOFT (HYDROPHILIC) CONTACT LENS, POWER PLUS (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS, SIMULVUE 38 (POLYMACON) SOFT (HYDROPHILIC) BIFOCAL CONTACT LENS and UNILENS 38 SOFT ASPHERIC CONTACT LENS.

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