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Angstrom Medica, Inc.

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Devices
1

What Angstrom Medica, Inc. makes

Angstrom Medica, Inc. manufactures the NanoSS Bone Void Filler, a material designed to fill and support bone defects during surgical procedures.

The NanoSS Bone Void Filler is classified as a Class II medical device under FDA regulations and is authorised 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

  • Nanoss Bone Void Filler Ref K050025

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

Frequently asked questions

How many devices does Angstrom Medica, Inc. have in the registry?

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

Which registries list Angstrom Medica, Inc.'s devices?

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

What risk classes do Angstrom Medica, Inc.'s devices fall under?

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

What are the newest devices from Angstrom Medica, Inc. in the registry?

The most recently registered devices listed for Angstrom Medica, Inc. include NANOSS BONE VOID FILLER.

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