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# FDA Clears Lensar Laser Expanded Presbyopia Treatment
- URL: https://www.fdaweb.com/fda-clears-lensar-laser-expanded-presbyopia-treatment/
- Published: 2018-04-11T12:00:00.000Z
- Updated: 2026-09-14T23:58:25.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141197

FDA has cleared a Lensar 510(k) for the Lensar Laser System with Streamline IV, that expands the platform’s capabilities to include the creation of the corneal pockets and flaps used in ophthalmic procedures treating presbyopia. The enhancement includes a new curved contact patient interface device that enables the creation of corneal pockets and flaps without compromising patient comfort, the company says. The laser system is cleared for anterior capsulotomy, lens fragmentation, corneal incisions including corneal pockets and flaps, and arcuate incisions.