# K252175: LANDR Contact LENS Case

- Pathway: 510(k) (Traditional)
- Applicant: Fourth Axis, LLC
- Decided: Feb 10, 2026 after 214 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
Longest line of descent: 6 generations back to K920064 (1992). 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)
- K240095: CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6), Shanghai Care US Medical Product Co., Ltd. (2024) Summary page 8.

## Indications for use
The LANDR Contact Lens Case is designed for storing soft (hydrophilic), rigid gas-permeable, and/or rigid contact lenses. It is only for use during storage with chemical disinfection and should not be used during heat disinfection.

Source page: https://510kreport.com/device/K252175
Methodology: https://510kreport.com/methodology