# K110566: Viberect Penile Vibratory Stimulation Device

- Pathway: 510(k) (Traditional)
- Applicant: Reflexonic, LLC
- Decided: Jun 24, 2011 after 116 days
- Product code: KXQ (Vibrator For Therapeutic Use, Genital)
- Device class: 2
- Regulation: 21 CFR 884.5960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K851646 (1985). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K851646: Vibrector, Multicept, Aps. (1985) Summary page 1.
- K955589: Ferticare Personal Therapeutic Vibrator, Multicept, Aps. (1996) Summary page 2.

## Most influential descendants
- K142304: Viberect Penile Vibratory Stimulation Device (2014), 0 descendants of its own

## Indications for use
ViberectT Penile Vibratory Stimulation Device is a hand held medical device indicated to provoke erections for men who experience erectile dysfunction and to provoke ejaculation for spinal cord injured men.

Source page: https://510kreport.com/device/K110566
Methodology: https://510kreport.com/methodology