Genesys Spine - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
Genesys Spine has 31 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Latest FDA clearance: Oct 2025. Active since 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Genesys Spine
31 devices
Cleared
Oct 22, 2025
SIros-X System
Orthopedic
89d
Cleared
Feb 07, 2025
Genesys Spine AIS-C II Cervical Interbody Fusion System
Orthopedic
170d
Cleared
Mar 29, 2024
Genesys Spine Sacroiliac Joint Fusion System with Navigation
Orthopedic
142d
Cleared
Dec 13, 2023
Genesys Spine 3DP AIS-C II Cervical Interbody System
Orthopedic
35d
Cleared
Mar 09, 2022
Genesys Spine 3DP Lumbar Interbody System
Orthopedic
56d
Cleared
Jan 08, 2020
Genesys Spine 3DP Cervical Interbody System
Orthopedic
218d
Cleared
Dec 12, 2019
Genesys Spine 3DP Lumbar Interbody System
Orthopedic
409d
Cleared
Oct 24, 2019
Genesys Spine Binary® Lumbar Plate System
Orthopedic
28d
Cleared
Sep 26, 2019
Genesys Spine Sacroiliac Joint Fusion System
Orthopedic
87d
Cleared
Aug 29, 2019
Binary® Anterior Cervical Plate System
Orthopedic
27d
Cleared
Aug 29, 2018
Genesys Spine AIS-C Cervical Stand-Alone System
Orthopedic
105d
Cleared
Apr 03, 2018
Genesys Spine Binary Lumbar Plate System
Orthopedic
103d