Lumos Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lumos Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Prismira
1
Total
1
Cleared
0
Denied
Lumos Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Lumos Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aepis Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Lumos Labs, Inc.
1 devices