Ceiba Healthcare US, Inc. is one of 25939 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceiba Healthcare US, Inc. - FDA 510(k) Cleared Devices
Recent clearances: eClinics
1
Total
1
Cleared
0
Denied
Ceiba Healthcare US, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ceiba Healthcare US, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ceiba Healthcare US, Inc.
1 devices