Clearance Summary
3nethra neo HD FA; 3nethra neo HD received FDA 510(k) clearance under submission number K243600, sponsored by Forus Health Pvt.Ltd. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2025-08-14.
- Submission: K243600
- Applicant / Sponsor: Forus Health Pvt.Ltd
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1120
- Decision date: 2025-08-14
Classification & Regulation
This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.