# Soflex Contact Lens Industries, Ltd.

- Location (FDA's records): Littleton, CO
- FDA decisions: 6 (2001–2004): 6 510(k) clearances
- Product codes: LPL (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K033655: Soflex Soft K (Xylofilcon a) Soft (Hydrophilic) Keratoconus Contact Lens for Daily Wear (Jul 30, 2004)
- K030842: Eni-Eye Q Toric (Acofilcon) Soft (Hydrophilic) Multifocal Contact Lens for Daily Wear, Eni-Eye (Acofilcon) Soft (Hydrop (Jun 6, 2003)
- K020642: Soft K. and Soft K. Toric (Xyloficon a) Soft (Hydrophillic) Keratoconus Contact Lens for Daily Wear (May 24, 2002)
- K013469: Eye-Q (Xylofilcon a) Soft (Hydrophilic) Multifocal Contact Lens for Daily Wear (Nov 20, 2001)
- K013467: Toric Eye-Q (Xylofilcon a) Soft (Hydrophilic) Toric Multifocal Contact Lens for Daily Wear (Nov 20, 2001)
- K011256: Toric Lite Lens (Jul 17, 2001)

Source page: https://510kreport.com/company/soflex-contact-lens-industries