Lesspine Innovations is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lesspine Innovations - FDA 510(k) Cleared Devices
Recent clearances: ELID (Endoscopic Less Invasive Decompression) System, Sacrix® Sacroiliac Joint Fusion Device System, Inspan® ScrewLES Fusion System, Invue® MAX™ + Invue Inset Anterior Cervical Plate System, and FacetFuse® Screw Fixation System
2
Total
2
Cleared
0
Denied
Lesspine Innovations has 2 FDA 510(k) cleared medical devices. Based in Malden, US.
Latest FDA clearance: Aug 2025. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Lesspine Innovations Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
FDA 510(k) Regulatory Record - Lesspine Innovations
2 devices