# K130285: Progent Large Diameter Contact Lens Case for Rigid Gas Permeable Lens

- Pathway: 510(k) (Traditional)
- Applicant: The Lagado Corp.
- Decided: Apr 3, 2013 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
Longest line of descent: 3 generations back to K002140 (2000). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991206: Bonasse Contact Lens Case, Bonasse Ent. Co., Ltd. (2000) Summary page 1.
- K122273: Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lens, Menicon Co, Ltd. (2013) Summary page 1.

## Indications for use
Menicon Progent Large Diameter Contact Lens Case is only intended for use with the Menicon Progent Protein Remover for Rigid Gas Permeable (RGP) Contact Lenses. The Menicon Progent Large Diameter Contact Lens Case provides an alternative lens case to hold large diameter lenses (11I mm to 23 mm) during the Menicon Progent Protein Remover treatment. The case is not intended for disinfection (chemical, heat or peroxide). The case is not intended for lens storage.

Source page: https://510kreport.com/device/K130285
Methodology: https://510kreport.com/methodology