K260507
- 510(k) number
- K260507
- Device name
- Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus
- Applicant
- INTEROJO, Inc. KR
- Product code
- LPL — Lenses, Soft Contact, Daily Wear
- Decision date
- 2026-05-29
- Date received
- 2026-02-17
- 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: K260507.pdf
Official FDA record: K260507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.