Medical Device Manufacturer · US , Charlottesville , VA

Luminoah - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026
1
Total
1
Cleared
0
Denied

Luminoah has 1 FDA 510(k) cleared medical devices. Based in Charlottesville, US.

Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Luminoah Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Luminoah
1 devices
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