Sibel Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sibel Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANNE Maternal, ANNE View, Central Hub, ANNE Chest
5
Total
5
Cleared
0
Denied
Sibel Health, Inc. has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Feb 2026. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sibel Health, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Sibel Health, Inc.
5 devices