Onkos Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Onkos Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ELEOS™ Limb Salvage System with NanoCept® Technology, My3D® Personalized Pelvic Reconstruction, ELEOS™ Bipolar Acetabular System
5
Total
5
Cleared
0
Denied
Onkos Surgical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Parsippany, US.
Latest FDA clearance: Jun 2026. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Onkos Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Onkos Surgical, Inc.
5 devices
Cleared
Jun 08, 2026
ELEOS™ with NanoCept® Technology Limb Salvage System
Orthopedic
259d
Cleared
Oct 15, 2025
ELEOS™ Limb Salvage System with NanoCept® Technology
Orthopedic
33d
Cleared
Jan 30, 2023
My3D® Personalized Pelvic Reconstruction
Orthopedic
89d
Cleared
Feb 23, 2018
ELEOS™ Bipolar Acetabular System
Orthopedic
37d
Cleared
Oct 28, 2016
ELEOS Limb Salvage System
Orthopedic
148d