Reflexonic, LLC is one of 5120 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.
Reflexonic, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Oct 03, 2014
Viberect Penile Vibratory Stimulation Device
Obstetrics & Gynecology
46d
Cleared
Jun 24, 2011
VIBERECT PENILE VIBRATORY STIMULATION DEVICE
Obstetrics & Gynecology
116d