Lima Corporate S.P.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lima Corporate S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: SMR Shoulder System, ArTT Augments and Buttresses and Bone Screws, SMR Reverse HP Shoulder System
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.
Regulatory submissions have been managed by Lima U.S.A., Inc., Peoples & Associates Consulting, LLC and Peoples & Associates - Stephen J. Peoples, Vmd, MS.
FDA 510(k) Regulatory Record - Lima Corporate S.P.A.
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