# K042562: Lens Plus Rewetting Drops

- Pathway: 510(k) (Abbreviated)
- Applicant: Advanced Medical Optics, Inc.
- Decided: Jul 29, 2005 after 311 days
- Product code: LPN (Accessories, Soft Lens Products)
- Device class: 2
- Regulation: 21 CFR 886.5928
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 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) Lens Plus® Rewetting Drops with the single-use vial: named in the summary without a submission number

## Most influential descendants
- K093367: Sterile Saline Solution (2010), 9 descendants of its own
- K110221: Eye-Cept Sterile Saline Solution (2011), 8 descendants of its own
- K151768: Menicon Saline Rinse Solution (2015), 6 descendants of its own
- K170483: Bausch + Lomb Sensitive Eyes Plus Saline Solution (2017), 2 descendants of its own
- K201069: VibrantVue Scleral Saline (2020), 1 descendant of its own

## Indications for use
Use LENS PLUS ® Rewetting Drops while wearing your lenses to moisten and rehydrate them. Also, use LENS PLUS ® Rewetting Drops to relieve minor irritation, discomfort and/or blurring which may occur while wearing your lenses.

Source page: https://510kreport.com/device/K042562
Methodology: https://510kreport.com/methodology