Exo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Lung AI (LAI001), Strain AI (SAI001), AI Platform (AIP001)
5
Total
5
Cleared
0
Denied
Exo, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Latest FDA clearance: Apr 2025. Active since 1983. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Exo, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Exo, Inc.
5 devices