LRX
- Product code
- LRX
- Device name
- Case, Contact Lens
- Device class
- Class 2
- 21 CFR
- 21 CFR 886.5928
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 82 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K252175 | 2026-02-10 | Fourth Axis, LLC | LANDR Contact LENS Case | |
| K250495 | 2025-08-01 | Avizor S.A. | MINI VP1 (PL67_F); MINI VP1 (PL61_F) | |
| K240095 | 2024-10-09 | Shanghai Care US Medical Product Co., … | CAREUS Contact Lens Case (Model 1, Model 2, Model 3,… |
Official FDA classification page: LRX
Classification and pathway per current FDA publications. Data from openFDA (CC0).