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Lesspine Innovations

FDA Regulatory Profile

Lesspine Innovations appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 27, 2025.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243774ELID (Endoscopic Less Invasive Decompression) SystemAugust 27, 2025
K232605Sacrix® Sacroiliac Joint Fusion Device System, Inspan® ScrewLES Fusion System, Invue® MAX™ + Invue ISeptember 28, 2023

FDA data resources