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Sb Lucius, Inc.

United StatesFDA applicant, unverified

Devices
15

What Sb Lucius, Inc. makes

Sb Lucius, Inc. makes orthopedic and spinal fixation devices, including the Lucius 76, Ceranum 50 and 90, Aigis-Plus, Aigis-PT, Aigis-XO, Aigis-Super, Aigis-Inlay, Aigis-A, Aigis-Soft, Neo 76, and Miracle 98 systems.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

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  • Lucius 76 Ref K023196

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

  • Ceranum 50 Ref K023199

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

  • Aigis-Plus Ref K024135

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

  • Aigis-Pt Ref K024144

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

  • Aigis-Xo Ref K024145

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

  • Aigis-Super Ref K024142

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

  • Neo 76 Ref K024141

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

  • Miracle 98 Ref K031010

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

  • Ceranum 90 Ref K023198

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

  • Aigis-Inlay Ref K024139

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

  • Aigis-A Ref K024140

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

  • Aigis-Soft Ref K024136

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

  • Ceranum 82 Ref K023197

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

  • Aigis-Fine Ref K024143

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

  • Ceranum 76 Ref K023200

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

Rows 1-15 of 15

Frequently asked questions

How many devices does Sb Lucius, Inc. have in the registry?

The registry currently lists 15 devices for Sb Lucius, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sb Lucius, Inc.'s devices?

Among its 15 most recently registered devices, Sb Lucius, Inc. has devices listed in FDA 510(k) (15 devices).

What risk classes do Sb Lucius, Inc.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for Sb Lucius, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sb Lucius, Inc. in the registry?

The most recently registered devices listed for Sb Lucius, Inc. include LUCIUS 76, CERANUM 50, AIGIS-PLUS and AIGIS-PT.

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