# Quantum Devices, Inc.

- Location (FDA's records): Grayslake, IL
- FDA decisions: 2 (2003–2012): 2 510(k) clearances
- Product codes: ILY (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 15 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Light Force Therapy, Inc.: 1 (https://510kreport.com/company/light-force-therapy)
- Bales Scientific, Inc.: 1 (https://510kreport.com/company/bales-scientific)
- Diomedics, Inc.: 1 (https://510kreport.com/company/diomedics)

## Firms that cite its devices most
- Biocare Systems, Inc.: 1 (https://510kreport.com/company/biocare-systems)
- H.V.R., Inc.: 1 (https://510kreport.com/company/hvr)
- Life Without Pain, LLC: 1 (https://510kreport.com/company/life-without-pain)
- Cottonwood Vessel Corporation: 1 (https://510kreport.com/company/cottonwood-vessel)
- Lynton Lasers Limited: 1 (https://510kreport.com/company/lynton-lasers)
- Genesis Health Light Corporation: 1 (https://510kreport.com/company/genesis-health-light)
- Home Skinovations, Ltd.: 1 (https://510kreport.com/company/home-skinovations)
- Atlantis Luminescent Products, LLC: 1 (https://510kreport.com/company/atlantis-luminescent-products)

## Its most-cited devices
- K032229: Quantum Warp 10 Light Delivery System (2003), cited by 15

## Recent decisions
- K113231: WARP10,WARP75 (Feb 27, 2012)
- K032229: Quantum Warp 10 Light Delivery System (Sep 12, 2003)

Source page: https://510kreport.com/company/quantum-devices