Alphatec Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alphatec Spine - FDA 510(k) Cleared Devices
Recent clearances: IdentiTi™ II ALIF Standalone Interbody System, IdentiTi Porous Ti Interbody System, Invictus Robotic Navigation Instruments
6
Total
6
Cleared
0
Denied
Alphatec Spine has 6 FDA 510(k) cleared medical devices. Based in Carlsnad, US.
Latest FDA clearance: Sep 2025. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Alphatec Spine Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alphatec Spine
6 devices
Cleared
Sep 03, 2025
IdentiTi™ II ALIF Standalone Interbody System
Orthopedic
104d
Cleared
Feb 03, 2025
IdentiTi Porous Ti Interbody System
Orthopedic
264d
Cleared
Jun 06, 2024
Invictus Robotic Navigation Instruments
Orthopedic
59d
Cleared
Oct 07, 2022
IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System,...
Orthopedic
88d
Cleared
Jun 03, 2019
Solanas® Posterior OCT Fixation System
Orthopedic
31d
Cleared
Sep 08, 2016
Battalion Universal Spacer System
Orthopedic
156d