Solius Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solius Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOLIUS PRO UVB Light Panel
1
Total
1
Cleared
0
Denied
Solius Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bainbridge Island, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Solius Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bentley Biomedical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Solius Labs, Inc.
1 devices