Spineology, Inc. - FDA 510(k) Cleared Devices
54
Total
51
Cleared
1
Denied
Spineology, Inc. has 51 FDA 510(k) cleared medical devices. Based in Stillwater, US.
Latest FDA clearance: Dec 2025. Active since 1999.
Browse the FDA 510(k) cleared devices submitted by Spineology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Spineology, Inc.
6 devices
Cleared
Dec 15, 2025
OptiMesh Multiplanar Expandable Interbody Fusion System
Orthopedic
231d
Cleared
Dec 04, 2025
Spineology Navigation Instruments
Orthopedic
163d
Cleared
Nov 01, 2023
OptiMesh Multiplanar Expandable Interbody Fusion System
Orthopedic
212d
Cleared
Oct 18, 2023
OptiMesh Multiplanar Expandable Interbody Fusion System
Orthopedic
124d
Cleared
Aug 05, 2022
Spineology Navigation Instruments
Orthopedic
235d
Cleared
Feb 19, 2021
Duo Expandable Interbody Fusion System
Orthopedic
29d