Reflexonic, LLC is one of 23331 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reflexonic, LLC - FDA 510(k) Cleared Devices
Recent clearances: Viberect Penile Vibratory Stimulation Device, VIBERECT PENILE VIBRATORY STIMULATION DEVICE
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.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Reflexonic, LLC
2 devices