# K915082: Opti-Lens (TM) Contact Lens Case

- Pathway: 510(k) (Traditional)
- Applicant: Ryder Intl. Corp.
- Decided: Jan 13, 1992 after 62 days
- Product code: LRX (Case, Contact Lens)
- 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K971618: Alcon Contact Lens Case (1997), 3 descendants of its own
- K974281: Alcon Contact Lens Case (1998), 2 descendants of its own
- K040914: Polyvial/Polypak, Contact Lens Case and Storage System Container for Ophthalmics (2004), 0 descendants of its own
- K032309: Novelens Contact Lens Cleaning Enhancement and Storage Accessory (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K915082
Methodology: https://510kreport.com/methodology