Luminance Medical Ventures, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Luminance Medical Ventures, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Luminance Red Cold Sore Device (TN1927G), The Luminance RED Acne Device
2
Total
2
Cleared
0
Denied
Luminance Medical Ventures, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Sep 2025. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Luminance Medical Ventures, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by leanRAQA, LLC and Medlaunch, LLC.
FDA 510(k) Regulatory Record - Luminance Medical Ventures, Inc.
2 devices