Orthonovis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cannulated Screw and Kirschner (K wire) System, BPS Wrist Fracture System, BPS - Bone Fragment Fixation Plates, Screws and Washers
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Orthonovis, Inc. Orthopedic ✕
5 devices
Cleared
Oct 02, 2025
Cannulated Screw and Kirschner (K wire) System
Orthopedic
34d
Cleared
Mar 17, 2025
BPS Wrist Fracture System
Orthopedic
25d
Cleared
Feb 06, 2025
BPS - Bone Fragment Fixation Plates, Screws and Washers
Orthopedic
27d
Cleared
Oct 04, 2024
BPS Wrist Fracture System
Orthopedic
58d
Cleared
Aug 25, 2022
ONX Large External Fixation System
Orthopedic
254d