# K053191: Discon Daily (Etafilcon a) One-Day Soft (Hydrophilic) Contact Lens

- Pathway: 510(k) (Special)
- Applicant: Innova Vision, Inc.
- Decided: May 12, 2006 after 178 days
- Product code: MVN (Lens, Contact, (Disposable))
- 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
Longest line of descent: 4 generations back to K962804 (1996). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051129: Discon (Etafilcon a) Soft (Hydrophilic) Contact Lens for Daily Wear, Innova Vision, Inc. (2005) Summary page 1.
- K013973: Acuvue Brand (Etafilcon a) Soft (Hydrophilic) Contact Lenses; Clear and Tinted (Visibility and/or Cosmetic) with UV Bloc, Vistakon (2002) Summary page 1.

## Indications for use
Discon Daily (Etafilcon A)One-Day Soft (hydrophilic) Contact Lens is indicated for the correction of visual acuity in not-aphakic persons with non-diseased eyes that are myopia or hyperopia and may exhibited refractive astigmatism up to 2.00 diopters that does not interfere with visual acuity. The eye care practitioner may prescribe the contact lens for single-use daily disposable wear. The Discon Daily Lenses are not intended to be disinfected and should be discarded after a single use.

Source page: https://510kreport.com/device/K053191
Methodology: https://510kreport.com/methodology