# K022266: Aurora SR

- Pathway: 510(k) (Traditional)
- Applicant: Syneron Medical, Ltd.
- Decided: Oct 3, 2002 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: 7 generations back to K943450 (1995). 32 ancestors in all.
705 later devices descend from it; 5 cite it directly.
0 of 738 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K950493: Photoderm VL., Esc, Energy Systems Corp. (1995) Summary page 1.
- K960772: Photoderm PL., Esc Medical Systems, Ltd. (1996) Summary page 1.
- K000944: Thermage Thermacool System, Thermage, Inc. (2000) Summary page 1.
- K982816: Vnus Closure System, Vnus Medical Technologies, Inc. (1999) Summary page 1.

## Most influential descendants
- K030426: Omnilux Red (2003), 563 descendants of its own
- K042630: Revlight Skin Care System (2005), 402 descendants of its own
- K031993: Aurora SR (2003), 303 descendants of its own
- K050452: Aurora SR and Sra Applicator (2005), 301 descendants of its own
- K053540: Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories That Are Used with Them to Deliver Laser Ene (2006), 299 descendants of its own

## Indications for use
The Aurora SR is indicated for treatment of superficial, benign vascular, and pigmented lesions.

Source page: https://510kreport.com/device/K022266
Methodology: https://510kreport.com/methodology