# K080300: Cutera Multimodal Cellulite Product (Cmmcd)

- Pathway: 510(k) (Traditional)
- Applicant: Cutera, Inc.
- Decided: Apr 8, 2008 after 63 days
- Product code: NUV (Massager, Vacuum, Light Induced Heating)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K943450 (1995). 57 ancestors in all.
101 later devices descend from it; 2 cite it directly.
0 of 159 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050397: Velasmooth, Shaper, Syneron Medical, Ltd. (2005) Summary page 1.
- K070092: Modification to Velasmooth, Shaper, Syneron Medical, Ltd. (2007) Summary page 1.
- K071872: Velashape, Syneron Medical, Ltd. (2007) Summary page 1.
- K030876: Cynosure Triactive Therapeutic Massage System, Cynosure, Inc. (2004) Summary page 1.
- K990445: LPG Therapeutic Massager, Models -Esi, Therapeutic Massager/Vibrator, Lpg USA, Inc. (2000) Summary page 1.

## Most influential descendants
- K090221: Reaction System (2009), 54 descendants of its own
- K082622: Alma Lasers Accent B-Shape Massager Handpiece/Module (2009), 45 descendants of its own
- K133837: Viora V-Total (2014), 33 descendants of its own
- K142093: V20 System (2014), 32 descendants of its own
- K150035: V10 system (2015), 31 descendants of its own

## Indications for use
The Cutera CMMCD infrared and RF energies are intended to provide topical heating for the purpose of elevating tissue temperature for the treatment of selected medical conditions such as relief of pain, muscle spasms, and increase in local circulation. The Cutera CMMCD massage device is intended to provide a temporary reduction in the appearance of cellulite.

Source page: https://510kreport.com/device/K080300
Methodology: https://510kreport.com/methodology