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Auxilium Biotechnologies, Inc.

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Devices
1

What Auxilium Biotechnologies, Inc. makes

Auxilium Biotechnologies, Inc. manufactures the NeuroSpan Bridge, a medical device designed for bridging spinal cord injuries to facilitate neural regeneration and connectivity.

The NeuroSpan Bridge is classified as a Class II 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • NeuroSpan Bridge Ref K253363

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

Frequently asked questions

How many devices does Auxilium Biotechnologies, Inc. have in the registry?

The registry currently lists 1 device for Auxilium Biotechnologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Auxilium Biotechnologies, Inc.'s devices?

Among its 1 most recently registered device, Auxilium Biotechnologies, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Auxilium Biotechnologies, Inc.'s devices fall under?

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

What are the newest devices from Auxilium Biotechnologies, Inc. in the registry?

The most recently registered devices listed for Auxilium Biotechnologies, Inc. include NeuroSpan Bridge.

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