CamDiab is one of 428 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
CamDiab - FDA 510(k) Cleared Devices
Recent clearances: iOS CamAPS FX
1
Total
1
Cleared
0
Denied
CamDiab has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by CamDiab Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MCRA,LLC as regulatory consultant. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - CamDiab
1 devices