Selux Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Selux Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PBC Separator with Selux AST System, PBC Separator with Selux AST System, Selux AST System
4
Total
4
Cleared
0
Denied
Selux Diagnostics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Charlestown, US.
Latest FDA clearance: Mar 2025. Active since 2023. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Selux Diagnostics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pbo Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Selux Diagnostics, Inc.
4 devices