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Landos, Inc.

United StatesFDA applicant, unverified

Devices
15

What Landos, Inc. makes

Landos, Inc. manufactures orthopedic fixation devices, including memory staples in multiple sizes, twist-off screws, and scarf thread-head screws designed for bone stabilization. Their portfolio also covers total hip prostheses, such as the Titanium Dysplastic Total Hip Prosthesis and the Morphometric Total Hip Prosthesis, along with femoral heads made from cobalt-chromium and zirconia. Additional products include the Nancy Nail for fracture fixation and the Euroform Total Hip Prosthesis, which is tailored for specific anatomical requirements.

The company’s devices are classified under Class II by the FDA and are authorised through the 510(k) clearance pathway. These products are listed in the FDA’s 510(k) registry, adhering to US regulatory standards for medical devices. Landos, Inc. is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

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  • Memory Staple (20 Sizes Available) Ref K964226

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

  • Twist-Off Screw Ref K962233

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

  • 34mm Scarf Thread-Head(Tm) Screw Ref K971068

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

  • Scarf Thread-Head Screw Ref K962236

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

  • Scarf Thread-Head (Tm) Head Screw Ref K971070

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

  • Titan Dysplasic Total Hip Prosthesis Ref K932935

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

  • Titan Trochantero-Diahyseal Total Hip Prosthesis Ref K933108

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

  • 22.2/+4MM Co Cr & Zirconia Femoral Head Ref K970846

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

  • Euroform Total Hip Prosthesis Ref K933567

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

  • Twist-Off (Tm) Screw Ref K971069

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

  • Nancy Nail Ref K960642

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

  • Morphometric Total Hip Prosthesis Ref K935185

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

  • Biostop G Bone Cement Restrictor Ref K943727 Open recall

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

  • Corail Ref K953111

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

  • Kar Ref K961732

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

Rows 1-15 of 15

Frequently asked questions

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

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

Which registries list Landos, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Landos, Inc. include MEMORY STAPLE (20 SIZES AVAILABLE), TWIST-OFF SCREW, 34MM SCARF THREAD-HEAD(TM) SCREW and SCARF THREAD-HEAD SCREW.

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