Centerline Biomedical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centerline Biomedical - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Centerline Biomedical has 1 FDA 510(k) cleared medical devices. Based in Warrensville Heights, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Centerline Biomedical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Centerline Biomedical
1 devices