U.S. Laser Worx is one of 4723 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U.S. Laser Worx - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
U.S. Laser Worx has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by U.S. Laser Worx Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U.S. Laser Worx
1 devices