# Magnivision, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 8 (1987–1990): 8 510(k) clearances
- Product codes: LRX (6), KYE (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K900778: Item #272 Magnif-Eyes Contact Lens Case (Mar 30, 1990)
- K900777: Item #273 Contact Lens Cases (Mar 30, 1990)
- K897084: Confees (R)+ Contact Lens Holder (Feb 28, 1990)
- K897085: Comfees (R) + Con-Pak (TM) Lens Case (Feb 28, 1990)
- K882384: Deluxe Contact Lens Holder (Hard & Soft) #283 (Jun 23, 1989)
- K890533: Item #352/#CS352* Contact Lens Cases (Jun 23, 1989)
- K872567: Soft Contact Lens Remover (Aug 10, 1987)
- K872591: Hard Contact Lens Remover. Item #289 (Aug 4, 1987)

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