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Vp Optics

South KoreaFDA 510(k) applicant, unverified

Devices
1

What Vp Optics makes

Vp Optics manufactures the AQUASPLASH Polymacon Soft (Hydrophilic) Daily Wear Contact Lens, designed for single-use, daily disposable eyewear.

This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Frequently asked questions

How many devices does Vp Optics have in the registry?

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

Which registries list Vp Optics's devices?

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

What risk classes do Vp Optics's devices fall under?

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

What are the newest devices from Vp Optics in the registry?

The most recently registered devices listed for Vp Optics include AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens.

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