CarboFix Orthopedics , Ltd. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
CarboFix Orthopedics , Ltd. has 32 FDA 510(k) cleared orthopedic devices. Based in Herzliya, IL.
Latest FDA clearance: Mar 2026. Active since 2011.
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 CarboFix Orthopedics , Ltd.
32 devices
Cleared
Mar 16, 2026
CarboClear® Posterior Cervical Screw System
Orthopedic
89d
Cleared
Nov 05, 2024
CarboClear® Hybrid Pedicle Screw System
Orthopedic
36d
Cleared
Aug 01, 2024
CarboClear® X Pedicle Screw System
Orthopedic
247d
Cleared
Apr 25, 2024
CarboClear® Hybrid Pedicle Screw System
Orthopedic
29d
Cleared
Mar 27, 2024
CarboClear® Posterior Cervical Screw System
Orthopedic
100d
Cleared
Jan 10, 2024
CarboClear® X Pedicle Screw System
Orthopedic
27d
Cleared
Oct 10, 2023
CarboClear® Pedicle Screw System
Orthopedic
67d
Cleared
Jul 03, 2023
CarboClear® X Pedicle Screw System
Orthopedic
61d
Cleared
Apr 06, 2021
CarboClear X Pedicle Screw System, CarboClear X Navigated Instruments
Orthopedic
27d
Cleared
Nov 25, 2020
CarboClear X Pedicle Screw System
Orthopedic
15d
Cleared
Oct 08, 2020
Piccolo Composite Proximal Tibia Plate System
Orthopedic
90d
Cleared
Aug 07, 2020
CarboClear® Pedicle Screw System, CarboClear® II Pedicle Screw System
Orthopedic
28d