OsteoCentric Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
OsteoCentric Technologies - FDA 510(k) Cleared Devices
Recent clearances: OsteoCentric® UnifiMI® TCS Plating System, The OsteoCentric Bone Plate and Screw System, OsteoCentric Technologies Cannulated Fasteners and Nuts
11
Total
11
Cleared
0
Denied
OsteoCentric Technologies has 11 FDA 510(k) cleared orthopedic devices. Based in Logan, US.
Latest FDA clearance: Aug 2025. Active since 2021.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp and Telos Partners, LLC.
FDA 510(k) Regulatory Record - OsteoCentric Technologies
11 devices
Cleared
Aug 16, 2025
OsteoCentric® UnifiMI® TCS Plating System
Orthopedic
54d
Cleared
Mar 18, 2025
The OsteoCentric Bone Plate and Screw System
Orthopedic
26d
Cleared
Oct 09, 2024
OsteoCentric Technologies Cannulated Fasteners and Nuts
Orthopedic
30d
Cleared
Oct 05, 2023
OsteoCentric Dental Implant System
Dental
248d
Cleared
Sep 21, 2023
Integrity-SI® Fusion System
Orthopedic
237d
Cleared
Jun 29, 2023
OsteoCentric ACL Fixation System
Orthopedic
118d
Cleared
Apr 18, 2023
OsteoCentric Integrated Hip Fastener System
Orthopedic
29d
Cleared
Sep 12, 2022
Integrity-SI Fusion System
Orthopedic
24d
Cleared
Jul 28, 2022
OsteoCentric Spine MIS Pedicle Fastener System
Orthopedic
80d
Cleared
Aug 03, 2021
Cannulated Fasteners and Nuts
Orthopedic
97d
Cleared
Apr 14, 2021
Cannulated Fasteners and Nuts
Orthopedic
30d