Orthonovis, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252758Cannulated Screw and Kirschner (K wire) SystemOctober 2, 2025
K250498BPS Wrist Fracture SystemMarch 17, 2025
K250055BPS - Bone Fragment Fixation Plates, Screws and WashersFebruary 6, 2025
K242343BPS Wrist Fracture SystemOctober 4, 2024
K213905ONX Large External Fixation SystemAugust 25, 2022