Reflexonic, LLC

FDA Regulatory Profile

Reflexonic, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 3, 2014.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142304Viberect Penile Vibratory Stimulation DeviceOctober 3, 2014
K110566VIBERECT PENILE VIBRATORY STIMULATION DEVICEJune 24, 2011