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# J&J Cataract Surgical Device Cleared
- URL: https://www.fdaweb.com/j-j-cataract-surgical-device-cleared/
- Published: 2021-04-21T12:00:00.000Z
- Updated: 2026-09-14T16:55:42.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149159

FDA has cleared a Johnson & Johnson Vision 510(k) for its next generation Veritas Vision System, a phacoemulsification (cataract surgery) device that allows surgeons to guide through any lens density with less surge and more stability, according to the company. The new system also is intended to improve ergonomics to further enhance usability during cataract surgery, it says. Phacoemulsification is the most common cataract surgery technique performed, J&J says, adding that it allows ophthalmologists to effectively emulsify and efficiently remove an eye’s internal lens when it has become cloudy from cataracts.