# Sunsoft Corp.

- Location (FDA's records): Albuquerque, NM
- FDA decisions: 2 (1995–1997): 2 510(k) clearances
- Product codes: LPL (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K964696: Sunsoft (Methafilcon a) Soft (Hydrophilic) Daily Wear Contact Lens (Feb 20, 1997)
- K942374: Allure (Methafilcon a) Soft (Hydrophilic) Daily Wear Contact Lens (Apr 13, 1995)

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