Serpex Medical, Inc. - FDA 510(k) Cleared Devices
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.
3 devices