Super Grow Lasers is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Super Grow Lasers - FDA 510(k) Cleared Devices
Recent clearances: SuperGrow 272, Ultimate 272
2
Total
2
Cleared
0
Denied
Super Grow Lasers has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Super Grow Lasers Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Super Grow Lasers
2 devices