Telesair, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Telesair, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AVEA disposable expiratory filter/water trap (11790), BONHAWA Respiratory Humidifier
2
Total
2
Cleared
0
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.
Regulatory submissions have been managed by ProMedic Consulting, LLC and ProMedic, LLC.
FDA 510(k) Regulatory Record - Telesair, Inc.
2 devices