Solius Labs, Inc. - FDA 510(k) Cleared Devices
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.
1 devices