Acurable Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Acurable Limited - FDA 510(k) Cleared Devices
Recent clearances: AcuPebble Ox (200), AcuPebble OX100, AcuPebble SA
3
Total
3
Cleared
0
Denied
Acurable Limited has 3 FDA 510(k) cleared medical devices. Based in London, GB.
Latest FDA clearance: Mar 2025. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Acurable Limited Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Acurable Limited
3 devices