Wesper, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Wesper, Inc. has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Apr 2026. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Wesper, Inc. Filter by specialty or product code using the sidebar.
4 devices