Medical Device Manufacturer · US , Irvine , CA

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

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Telesair, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.

Latest FDA clearance: May 2025. Active since 2023. Primary specialty: Anesthesiology.

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

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

2 devices

1-2 of 2