Lespine Innovations, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lespine Innovations, LLC - FDA 510(k) Cleared Devices
Recent clearances: Inspan ScrewLES Fusion System
1
Total
1
Cleared
0
Denied
Lespine Innovations, LLC has 1 FDA 510(k) cleared medical devices. Based in Malden, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Lespine Innovations, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRCA, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Lespine Innovations, LLC
1 devices