Serpex Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Serpex Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01, Compass Steerable Needle, Recon Steerable Sheath
3
Total
3
Cleared
0
Denied
Serpex Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Latest FDA clearance: Oct 2025. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Serpex Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Honkanen Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Serpex Medical, Inc.
3 devices