Tyber Medical, LLC is one of 12883 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyber Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Exalta Proximal Tibia Plating System, Anteralign LS coverplate, Navigated LLIF Impactable Tracker
31
Total
31
Cleared
0
Denied
Tyber Medical, LLC has 31 FDA 510(k) cleared orthopedic devices. Based in Morristown, US.
Latest FDA clearance: Jun 2026. Active since 2013.
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) Regulatory Record - Tyber Medical, LLC
31 devices
Cleared
Jun 12, 2026
Exalta Proximal Tibia Plating System
Orthopedic
60d
Cleared
Jun 10, 2026
Anteralign LS coverplate
Orthopedic
90d
Cleared
May 29, 2026
Navigated LLIF Impactable Tracker
Orthopedic
59d
Cleared
Apr 03, 2026
Tyber Medical Trauma Screw
Orthopedic
193d
Cleared
Dec 31, 2025
Tyber Medical Trauma Screw
Orthopedic
111d
Cleared
Oct 28, 2025
Navigated Instruments
Orthopedic
61d
Cleared
Jul 30, 2025
Tyber Medical Distal Radius Plating System
Orthopedic
90d
Cleared
Mar 19, 2025
Tyber Medical Anatomical Plating System
Orthopedic
210d
Cleared
May 31, 2024
Tyber Medical Anatomical Plating System
Orthopedic
30d
Cleared
Dec 21, 2023
Tyber Medical Anatomical Plating System – Line extension to the Mini-Frag System
Orthopedic
72d
Cleared
Dec 20, 2023
TM Plating System
Orthopedic
89d
Cleared
Dec 13, 2023
Anatomical Plating System (various)
Orthopedic
104d