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Reflexonic, LLC

FDA Regulatory Profile

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