Xstrahl, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Xstrahl, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: XBeam (v2), X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)
3
Total
3
Cleared
0
Denied
Xstrahl, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Brownhills, GB.
Latest FDA clearance: Dec 2024. Active since 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Xstrahl, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xstrahl, Ltd.
3 devices