Limacorporate is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Limacorporate - FDA 510(k) Cleared Devices
Recent clearances: Biolox® Delta Revision heads, SMR TT Hybrid Glenoid, SMR 3-Pegs Cemented Glenoid, Physica LMC Knee System
4
Total
4
Cleared
0
Denied
Limacorporate has 4 FDA 510(k) cleared medical devices. Based in San Daniele Del Friuli, IT.
Latest FDA clearance: Mar 2025. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Limacorporate Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lima U.S.A., Inc., Musculoskeletal Clinical Regulatory Advisers, LLC and Enovis.
FDA 510(k) Regulatory Record - Limacorporate
4 devices