Medical Device Manufacturer · US , Logan , UT

OsteoCentric Technologies - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2021
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
1-11 of 11
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