# Mi Gwang Contact Lens Co., Ltd.

- Location (FDA's records): Grand Junction, CO
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: LPL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Joowon Innovation Co., Ltd.: 1 (https://510kreport.com/company/joowon-innovation)
- Neo Vision Co., Ltd.: 1 (https://510kreport.com/company/neo-vision)
- The See Clear Company, Inc.: 1 (https://510kreport.com/company/see-clear)
- Vassen Co., Ltd.: 1 (https://510kreport.com/company/vassen)
- Dreamcon Co., Ltd.: 1 (https://510kreport.com/company/dreamcon)

## Its most-cited devices
- K051477: Migwang Comfort 38 (Polymacon) Spherical and Toric Soft Contact Lens for Daily Wear (Clear, Tinted and Cosmetic) (2006), cited by 5

## Recent decisions
- K051477: Migwang Comfort 38 (Polymacon) Spherical and Toric Soft Contact Lens for Daily Wear (Clear, Tinted and Cosmetic) (Mar 10, 2006)

Source page: https://510kreport.com/company/mi-gwang-contact-lens
