# K123474: Avant Laser

- Pathway: 510(k) (Abbreviated)
- Applicant: Avant Wellness Systems, LLC
- Decided: Dec 3, 2013 after 385 days
- Product code: ILY (Lamp, Infrared, Therapeutic Heating)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Avant Laser Model 1Z30 and 1Z30-X are intended to emit energy in the visible and near Infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for a temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and the temporary relaxation of muscles.

Source page: https://510kreport.com/device/K123474
Methodology: https://510kreport.com/methodology