Xiros Plc is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Xiros Plc - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Xiros Plc has 2 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Xiros Plc Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xiros Plc
2 devices