Respinova, Ltd. - FDA 510(k) Cleared Devices

Respinova, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Herzliya, IL.

Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Respinova, Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Ironstone Product Development, Inc. as regulatory consultant.