# K920064: Opti-Lens Contact Lens Case

- Pathway: 510(k) (Traditional)
- Applicant: Ryder Intl. Corp.
- Decided: Mar 4, 1992 after 57 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.
24 later devices descend from it; 1 cites it directly.
0 of 25 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
- K042578: I-Promotions Contact Lens Case (2005), 23 descendants of its own
- K071081: Contact Lens Case (2007), 17 descendants of its own
- K093377: Polaris Contact Lens Case (2010), 11 descendants of its own
- K120904: Polaris Dial-a-Date Contact Lens Case (2012), 9 descendants of its own
- K130930: Owl Contact Lens Cases, Dog Contact Lens Cases (2014), 5 descendants of its own

Source page: https://510kreport.com/device/K920064
Methodology: https://510kreport.com/methodology