Onkos Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Onkos Surgical - FDA 510(k) Cleared Devices
Recent clearances: My3D® Personalized Pelvic Reconstruction, ELEOS Limb Salvage System, ELEOS Limb Salvage System with BioGrip
6
Total
5
Cleared
1
Denied
Onkos Surgical has 5 FDA 510(k) cleared medical devices. Based in Parsippany, US.
Last cleared in 2022. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Onkos Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Onkos Surgical
6 devices
Not Cleared
Apr 05, 2024
ELEOSx™ Limb Salvage System
Orthopedic
827d
Cleared
Jul 06, 2022
My3D® Personalized Pelvic Reconstruction
Orthopedic
306d
Cleared
Jul 28, 2021
ELEOS Limb Salvage System
Orthopedic
57d
Cleared
Jun 09, 2021
ELEOS Limb Salvage System with BioGrip
Orthopedic
162d
Cleared
Feb 05, 2021
ELEOS™ Limb Salvage System
Orthopedic
59d
Cleared
Dec 11, 2020
ELEOS Limb Salvage System featuring BIOGRIP
Orthopedic
59d