Clearance Summary
Pegavision (Hioxifilcon A) Daily Disposable Soft Contact Lenses received FDA 510(k) clearance under submission number K251095, sponsored by Pegavision Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2025-09-17.
- Submission: K251095
- Applicant / Sponsor: Pegavision Corporation
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5925
- Decision date: 2025-09-17
Classification & Regulation
This clearance is catalogued under FDA product code LPL and 21 CFR 886.5925, within the Ophthalmic review panel as a Class II device.