Medical Device Manufacturer · US , New York , NY

Wesper, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2021

Total

Cleared

Denied

Wesper, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2023. 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.

FDA 510(k) cleared devices by Wesper, Inc.

3 devices

1-3 of 3