Osteocentric Technologies D.B.A. Osteocentric Trauma is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteocentric Technologies D.B.A. Osteocentric Trauma - FDA 510(k) Cle...
Recent clearances: OsteoCentric Integrated Hip Fastener System
1
Total
1
Cleared
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Denied
Osteocentric Technologies D.B.A. Osteocentric Trauma has 1 FDA 510(k) cleared medical devices. Based in Logan, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteocentric Technologies D.B.A. Osteocentric Trauma Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Osteocentric Technologies D.B.A. Osteocentric Trauma
1 devices