# K021720: Multivision Methafilcon a Soft (Hydropilic) Multifocal Lens for Daily Wear

- Pathway: 510(k) (Traditional)
- Applicant: Soflex Isralens Contact Lens, Ltd.
- Decided: Aug 12, 2002 after 80 days
- Product code: LPL (Lenses, Soft Contact, Daily Wear)
- Device class: 2
- Regulation: 21 CFR 886.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The MULTIVISION (methafilcon A) Soft (hydrophilic) Multifocal Contact Lens for Daily Wear is indicated for daily wear for the correction of refractive ametropia (myopia and hyperopia) and presbyopia in aphakic and not-aphakic persons with non-diseased eyes that may exhibit refractive and/or corneal astigmatism up to 0.75 diopters. The lens may be disinfected using a chemical disinfection system.

Source page: https://510kreport.com/device/K021720
Methodology: https://510kreport.com/methodology