Medical Device Manufacturer · US , Winona Lake , IN

Lima Corporate S.P.A. - FDA 510(k) Cleared Devices

64 submissions · 64 cleared · Since 2011

Total

Cleared

Denied

Lima Corporate S.P.A. has 64 FDA 510(k) cleared orthopedic devices. Based in Winona Lake, US.

Latest FDA clearance: Jan 2026. Active since 2011.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Lima Corporate S.P.A.

64 devices

1-12 of 64

ArTT Augments and Buttresses and Bone Screws

K251718 · LPH

Orthopedic · 86d

Cleared Jul 03, 2025

SMR Reverse HP Shoulder System

K243826 · PHX

Orthopedic · 203d

Cleared May 22, 2025

Physica System (Physica CR Porous Femoral components)

K250980 · MBH

Orthopedic · 52d

Cleared Dec 18, 2024

Physica Porous Femoral Components

SMR Hybrid Glenoid System

SMR Stemless Anatomic

Smart SPACE Shoulder Planner and 3D Positioners

K222405 · QHE

Orthopedic · 133d

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Lima Corporate S.P.A. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Lima Corporate S.P.A.

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