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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
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
CT
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