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Alacer Biomedical, Inc.

Country not established

Devices
1

What Alacer Biomedical, Inc. makes

Alacer Biomedical, Inc. manufactures the ALACER Surgical Scaffold, a medical device designed to support tissue integration and structural reinforcement in surgical procedures.

The ALACER Surgical Scaffold is classified as a Class II device under FDA regulations and is 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

  • Alacer Surgical Scaffold Ref K103445

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

Frequently asked questions

How many devices does Alacer Biomedical, Inc. have in the registry?

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

Which registries list Alacer Biomedical, Inc.'s devices?

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

What risk classes do Alacer Biomedical, Inc.'s devices fall under?

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

What are the newest devices from Alacer Biomedical, Inc. in the registry?

The most recently registered devices listed for Alacer Biomedical, Inc. include ALACER SURGICAL SCAFFOLD.

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