Tissue Regenix Group Plc is one of 167 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Tissue Regenix Group Plc - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Tissue Regenix Group Plc has 1 FDA 510(k) cleared medical devices. Based in York, GB.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tissue Regenix Group Plc Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tissue Regenix Group Plc
1 devices