FDA 510(k) Applications Submitted by REFLEXONIC, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110566 | 02/28/2011 | VIBERECT PENILE VIBRATORY STIMULATION DEVICE | REFLEXONIC, LLC |
| K142304 | 08/18/2014 | Viberect Penile Vibratory Stimulation Device | REFLEXONIC, LLC |
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