# K022888: Acubeam, Super Nova, Dio

- Pathway: 510(k) (Traditional)
- Applicant: Light Force Therapy, Inc.
- Decided: Dec 11, 2002 after 103 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.
201 later devices descend from it; 8 cite it directly.
0 of 202 devices 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.

## Most influential descendants
- K032229: Quantum Warp 10 Light Delivery System (2003), 198 descendants of its own
- K043317: Omnilux Plus (2005), 171 descendants of its own
- K050216: Omnilux Revive and Omnilux Plus (2005), 160 descendants of its own
- K060792: Illumimed (2006), 115 descendants of its own
- K083183: Aklarus Phototherapy System (2009), 91 descendants of its own

## Indications for use
The Light-Force-Therapy line of infrared lamps are indicated for use to emit energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature, for the temporary relief of minor muscle and joint pain, arthritis and muscle spasm; relieving stiffness; promoting relaxation of muscle tissue; and to temporarily increase local blood circulation where applied

Source page: https://510kreport.com/device/K022888
Methodology: https://510kreport.com/methodology