Stabilix, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stabilix, LLC - FDA 510(k) Cleared Devices
Recent clearances: AerFrame Patient Immobilization System (AFPIS)
1
Total
1
Cleared
0
Denied
Stabilix, LLC has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Stabilix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stabilix, LLC
1 devices