Prolaio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prolaio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: prolaio eVO2peak Module (Version 1.0)
1
Total
1
Cleared
0
Denied
Prolaio, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Prolaio, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Prolaio, Inc.
1 devices