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Exogenesis Corporation

Country not established

Devices
1

What Exogenesis Corporation makes

Exogenesis Corporation manufactures the Exogenesis Hernia Mesh, a Class II medical device.

The company is based in the US and its hernia mesh is listed in the FDA 510(k) registry.

AI-generated from registry data, 26 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Exogenesis Hernia Mesh Ref K191545

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Exogenesis Corporation have in the registry?

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

Which registries list Exogenesis Corporation's devices?

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

What risk classes do Exogenesis Corporation's devices fall under?

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

What are the newest devices from Exogenesis Corporation in the registry?

The most recently registered devices listed for Exogenesis Corporation include Exogenesis Hernia Mesh.

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