# K102494: The Buzz Facial Toning System

- Pathway: 510(k) (Traditional)
- Applicant: Daka International, Ltd.
- Decided: Dec 9, 2011 after 465 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K951951 (1996). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011935: Rejuvenique Model #RJV10, Salton, Inc. (2001) Summary page 1.
- K040871: Facemaster Facial Toning System, Facemaster of Beverly Hills, Inc. (2005) Summary page 1.
- K072260: Nuface, Model NU-4003, Carol Cole Company (2007)
- K070217: Interx 1000/Derma 200 Stimulator for Cosmetic Use, Neuro Resource Group, Inc. (2008) Summary page 1.
- K070250: Nutritone Facial Beauty System, Isomers Laboratories, Inc. (2008) Summary page 1.
- K071573: Rugalift, Model# V.2.1, Fatrotek S.R.L. (2008) Summary page 1.

## Indications for use
The Beauty Buzz Facial Toning System is indicated for cosmetic use.

Source page: https://510kreport.com/device/K102494
Methodology: https://510kreport.com/methodology