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Allergan Optical

Country not established

Devices
2

What Allergan Optical makes

Allergan Optical manufactures contact lens care products, including a daily lens cleaner and a lens case designed for single-use or reusable contact lenses.

These products are classified as Class II medical devices 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.

Catalogue2

Newest first, rows 1-2 of 2

  • Duraclean Daily Cleaner Ref K881987

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Allergan Lens Case Ref K884251

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

Frequently asked questions

How many devices does Allergan Optical have in the registry?

The registry currently lists 2 devices for Allergan Optical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Allergan Optical's devices?

Among its 2 most recently registered devices, Allergan Optical has devices listed in FDA 510(k) (2 devices).

What risk classes do Allergan Optical's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Allergan Optical's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Allergan Optical in the registry?

The most recently registered devices listed for Allergan Optical include DURACLEAN DAILY CLEANER and ALLERGAN LENS CASE.

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