K252175
- 510(k) number
- K252175
- Device name
- LANDR Contact LENS Case
- Applicant
- Fourth Axis, LLC ID · US
- Product code
- LRX — Case, Contact Lens
- Decision date
- 2026-02-10
- Date received
- 2025-07-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252175.pdf
Official FDA record: K252175
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.