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Lacerta Life Sciences

Also registered as Lacerta Life Science

Country not established

Devices
2

What Lacerta Life Sciences makes

Lacerta Life Sciences manufactures the LacertaMatrix, a medical device designed for tissue engineering and regenerative applications, intended to support cellular attachment and growth in controlled environments.

The LacertaMatrix is classified as a Class II (U) 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • LacertaMatrix Ref K252673

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

  • LacertaMatrix Ref K260218

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

Frequently asked questions

How many devices does Lacerta Life Sciences have in the registry?

The registry currently lists 2 devices for Lacerta Life Sciences. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lacerta Life Sciences's devices?

Among its 2 most recently registered devices, Lacerta Life Sciences has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Lacerta Life Sciences in the registry?

The most recently registered devices listed for Lacerta Life Sciences include LacertaMatrix.

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