# K961428: Soft-55 Daily Wear Contact Lens

- Pathway: 510(k) (Traditional)
- Applicant: Lombart Lenses, Ltd.
- Decided: May 21, 1996 after 36 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Softcon® Daily Wear lens: named in the summary without a submission number

## Most influential descendants
- K110452: Sof-Form II, Unilens, Unisite, Simulvue, Aquaflex, LL-38, Bayvue Aquaflex Mto, Unilens 38, Unisoft, Simulvue 38 Llbi 2, (2011), 0 descendants of its own

## Indications for use
they are fit on the comea to correct the vision acuity of the patient.

Source page: https://510kreport.com/device/K961428
Methodology: https://510kreport.com/methodology