Saranas, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Saranas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Saranas Early Bird Bleed Monitoring System
2
Total
1
Cleared
1
Denied
Saranas, Inc. has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Last cleared in 2023. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Saranas, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Saranas, Inc.
2 devices