Stabiliz Orthopaedics, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Stabiliz Orthopaedics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Exton, US.
Latest FDA clearance: Mar 2026. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stabiliz Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and MCRA.
2 devices