Stabiliz Orthopaedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stabiliz Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QuikFix External Fixator: Knee-Spanning Pack, SimpliFix Hip System
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.
FDA 510(k) Regulatory Record - Stabiliz Orthopaedics, Inc.
2 devices