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Keratec Limited

Country not established

Devices
1

What Keratec Limited makes

Keratec Limited manufactures Keratec wound dressings, designed for the management of corneal wounds and ocular surface injuries.

These products are classified as Class II (U) 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Keratec Wound Dressings Ref K080949

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

Frequently asked questions

How many devices does Keratec Limited have in the registry?

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

Which registries list Keratec Limited's devices?

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

What are the newest devices from Keratec Limited in the registry?

The most recently registered devices listed for Keratec Limited include KERATEC WOUND DRESSINGS.

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