Reflexonic, LLC is one of 5630 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reflexonic, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Reflexonic, LLC has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 2011 to 2014. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Reflexonic, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reflexonic, LLC
2 devices