# Reflexonic, LLC

- Location (FDA's records): Austin, TX
- FDA decisions: 2 (2011–2014): 2 510(k) clearances
- Product codes: KXQ (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Multicept, Aps.: 2 (https://510kreport.com/company/multicept)

## Its most-cited devices
- K110566: Viberect Penile Vibratory Stimulation Device (2011), cited by 1

## Recent decisions
- K142304: Viberect Penile Vibratory Stimulation Device (Oct 3, 2014)
- K110566: Viberect Penile Vibratory Stimulation Device (Jun 24, 2011)

Source page: https://510kreport.com/company/reflexonic