# KXQ: Vibrator For Therapeutic Use, Genital

- Device class: 2; regulation: 21 CFR 884.5960; FDA's rule: 510(k) exempt
- FDA decisions: 4
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1996: 1
- 2001: 1
- 2011: 1
- 2014: 1

## Most-cited predicates
- K955589: Ferticare Personal Therapeutic Vibrator (1996), cited by 1
- K110566: Viberect Penile Vibratory Stimulation Device (2011), cited by 1

Source page: https://510kreport.com/product-code/KXQ
Data by year (CSV): https://510kreport.com/product-code/KXQ.csv