Neurolign USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurolign USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: I-Portal Neuro Otologic Test Center, I-Portal Video Nystagmography System, I-Portal Portable Assessment System - Nysragmograph
1
Total
1
Cleared
0
Denied
Neurolign USA, LLC has 1 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neurolign USA, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Neurolign USA, LLC
1 devices