# K063249: Beamax

- Pathway: 510(k) (Traditional)
- Applicant: Medic Sharplight, Ltd.
- Decided: Jan 17, 2007 after 83 days
- Product code: GEX (Powered Laser Surgical Instrument)
- 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: 8 generations back to K910422 (1992). 86 ancestors in all.
58 later devices descend from it; 1 cites it directly.
0 of 145 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033946: Lovely System, Msq (M2), Ltd. (2004) Summary page 1.

## Most influential descendants
- K082876: Beamax/ Formax Pulsed Light Device Family (2008), 57 descendants of its own
- K111303: Dermatological Treatment Device Family (2011), 56 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 BEAMAX is intended for aesthetic and cosmetic use. The device is specifically indicated for removal of hair by using selective light energy.

Source page: https://510kreport.com/device/K063249
Methodology: https://510kreport.com/methodology