KXQ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Vibrator For Therapeutic Use, Genital
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.5960
- Medical specialty
- Obstetrics/Gynecology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Viberect Penile Vibratory Stimulation Device (K142304) | Reflexonic, LLC | 2014-10-03 |
| VIBERECT PENILE VIBRATORY STIMULATION DEVICE (K110566) | Reflexonic, LLC | 2011-06-24 |
| MULTI CARE THERAPEUTIC VIBRATOR (K010096) | Multicept A/S | 2001-03-05 |
| FERTICARE PERSONAL THERAPEUTIC VIBRATOR (K955589) | Multicept, Aps. | 1996-04-11 |
Track KXQ automatically
Every clearance here is in the API, with alerts when new ones post.