# Curelight, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 6 (2002–2004): 6 510(k) clearances
- Product codes: GEX (6)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 13 (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)
- Medx Electronics, Inc.: 1 (https://510kreport.com/company/medx-electronics)
- C&H International: 1 (https://510kreport.com/company/c-h-international)

## Firms that cite its devices most
- Photo Therapeutics Limited: 2 (https://510kreport.com/company/photo-therapeutics)
- Msq (M2), Ltd.: 2 (https://510kreport.com/company/msq-m2)
- Spectragenics, Inc.: 2 (https://510kreport.com/company/spectragenics)
- Bhc International, Ltd.: 1 (https://510kreport.com/company/bhc-international)
- Skincare Technology, Inc.: 1 (https://510kreport.com/company/skincare-technology)
- Syneron Medical, Ltd.: 1 (https://510kreport.com/company/syneron-medical)
- Transverse Industries Co.: 1 (https://510kreport.com/company/transverse-industries)
- Care Electronics, Inc.: 1 (https://510kreport.com/company/care-electronics)

## Its most-cited devices
- K013623: Clearlight Phototheraphy System, Model CL 420 (2002), cited by 10
- K030338: Iclear Phototherapy System, Model FGCM0002 (2003), cited by 3

## Recent decisions
- K041994: Multiclear XL Multiwavelength Targeted Phototherapy System (Oct 6, 2004)
- K041569: CLEAR100 Phototherapy System, Model FGCM0002 (Jun 30, 2004)
- K033183: Reclear Phototherapy System, Model FGCM0012 (Apr 15, 2004)
- K032383: Multiclear Multiwavelength Targeted Phototherapy System (Nov 28, 2003)
- K030338: Iclear Phototherapy System, Model FGCM0002 (Feb 12, 2003)
- K013623: Clearlight Phototheraphy System, Model CL 420 (Aug 16, 2002)

Source page: https://510kreport.com/company/curelight