Corvent Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corvent Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CorVision® (91-205-Z0014), RESPOND(R) Ventilator
2
Total
2
Cleared
0
Denied
Corvent Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fargo, US.
Latest FDA clearance: May 2026. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Corvent Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by ProMedic, LLC and CorVent® Medical, Inc..
FDA 510(k) Regulatory Record - Corvent Medical, Inc.
2 devices