Medical Device Manufacturer · IL , Binyamina

Hospitech Respiration , Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2010

Total

Cleared

Denied

Hospitech Respiration , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Binyamina, IL.

Last cleared in 2022. Active since 2010. Primary specialty: Anesthesiology.

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

Regulatory submissions have been managed by Qsite and ProMedoss, Inc..

Hospitech Respiration , Ltd. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hospitech Respiration , Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 18, 2026