Retropsoas Technologies, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Retropsoas Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Frontenac, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Retropsoas Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Retropsoas Technologies, LLC
2 devices