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Lucens Technology Co., Ltd.

TaiwanFDA applicant, unverified

Devices
1

What Lucens Technology Co., Ltd. makes

Lucens Technology Co., Ltd. produces the Lucens 41, a silicone hydrogel soft contact lens made of senofilcon C material, which is hydrophilic.

The Lucens 41 is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the US.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Lucens Technology Co., Ltd. have in the registry?

The registry currently lists 1 device for Lucens Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lucens Technology Co., Ltd.'s devices?

Among its 1 most recently registered device, Lucens Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Lucens Technology Co., Ltd.'s devices fall under?

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

What are the newest devices from Lucens Technology Co., Ltd. in the registry?

The most recently registered devices listed for Lucens Technology Co., Ltd. include Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens.

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