Proscia, Inc. is one of 16294 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Proscia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Concentriq AP-Dx, Concentriq Dx
2
Total
2
Cleared
0
Denied
Proscia, Inc. has 2 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Latest FDA clearance: Aug 2026. Active since 2024. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Proscia, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Proscia, Inc.
2 devices