Spiway, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spiway, LLC - FDA 510(k) Cleared Devices
Recent clearances: SPIWay Endonasal Access Guide, SPIWay Endonasal Access Guide
4
Total
4
Cleared
0
Denied
Spiway, LLC has 4 FDA 510(k) cleared medical devices. Based in Laguna Beach, US.
Last cleared in 2021. Active since 2014. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Spiway, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spiway, LLC
4 devices