Centerline Biomedical is one of 16249 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centerline Biomedical - FDA 510(k) Cleared Devices
Recent clearances: Intra-Operative Positioning System (IOPS) and IOPS Visionary System, Intra-Operative Positioning System (IOPS) (MC-1)
2
Total
2
Cleared
0
Denied
Centerline Biomedical has 2 FDA 510(k) cleared medical devices. Based in Warrensville Heights, US.
Latest FDA clearance: Oct 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
2 devices