Medovate Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Medovate Limited - FDA 510(k) Cleared Devices
Recent clearances: SAFIRA
1
Total
1
Cleared
0
Denied
Medovate Limited has 1 FDA 510(k) cleared medical devices. Based in Girton, GB.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medovate Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Delphi Medical Device Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medovate Limited
1 devices