VisionAir Solutions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
VisionAir Solutions - FDA 510(k) Cleared Devices
Recent clearances: VisionAir Enhanced Stock Stent
1
Total
1
Cleared
0
Denied
VisionAir Solutions has 1 FDA 510(k) cleared medical devices. Based in Akron, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by VisionAir Solutions Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - VisionAir Solutions
1 devices