Lighthouse Technical Innovations, Inc. is one of 21641 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lighthouse Technical Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EXPANDED SPECTRUM PHOTO THERAPY DEVICE, MODEL ESPT-3X
1
Total
1
Cleared
0
Denied
Lighthouse Technical Innovations, Inc. has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Lighthouse Technical Innovations, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Lighthouse Technical Innovations, Inc.
1 devices