Fourth Axis, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Fourth Axis, LLC has 1 FDA 510(k) cleared medical devices. Based in Boise, US.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Fourth Axis, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bdra Consulting, LLC as regulatory consultant.
1 devices