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Lima Corporate S.p.A.

Country not established FDA

Devices
64
Registrations
FDA
FDA recalls
0

What Lima Corporate S.p.A. makes

Lima Corporate S.P.A. manufactures orthopedic implants for shoulder, hip, and knee replacements, including reverse shoulder systems (e.g., SMR Reverse Shoulder, PRIMA Humeral/Glenoid), femoral stems (e.g., MASTERSL, H-MAX S), acetabular systems (e.g., Delta TT), and knee prosthetics (e.g., Physica PS). Their portfolio also includes modular components like augments, buttresses, and bone screws (ArTT series), as well as glenoid implants (SMR 3-Pegs) and planning tools (Smart SPACE Shoulder Planner).

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device authorization requirements. Lima Corporate S.P.A. operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue64

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  • MasterSL femoral stem Ref K143509

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

  • SMR TT Augmented Glenoid System Ref K200171

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

  • PRIMA Humeral System and SMR Glenosphere Ø42 Ref K212800 Open recall

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

  • SMR Hybrid Glenoid System Ref K163397 Open recall

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

  • SMR Modular Glenoid Ref K143256

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

  • Delta Tt Cups, Delta Tt Liners, Bone Screws Ref K112898

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

  • H-Max S stem Ref K160011

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

  • SMR 140° Reverse Humeral Body Ref K201905

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

  • AMF Revision TT Cones Ref K200653

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

  • Smr Tt Metal Back Glenoid Ref K133349

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

  • SMR Hybrid Glenoid System Ref K231099

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

  • TEMA Elbow system - Line extension Ref K222807 Open recall

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

  • Physica LMC Knee System Ref K193284

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

  • Physica CR Knee System Ref K151266

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

Rows 51-64 of 64

Showing 51-64 of 64

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • LIMACORPORATE S.p.A. Villanova di San Daniele Udine · IT FEI 3008021110