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# FDA Clears Bausch + Lomb Vitesse Device
- URL: https://www.fdaweb.com/fda-clears-bausch-lomb-vitesse-device/
- Published: 2017-04-26T12:00:00.000Z
- Updated: 2026-09-14T22:20:07.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5138548

FDA has cleared a Bausch + Lomb 510(k) for Vitesse, a hypersonic device for vitreous removal. The device features a single-needle design and a continuously open-port system. It will exclusively operate on the company’s new Stellaris Elite Vision Enhancement System, the company’s next generation phacoemulsification cataract platform (see earlier story).