B+L Receives FDA Clearance for Vitesse Vitrectomy System

 B+L Receives FDA Clearance for Vitesse Vitrectomy System

Bausch + Lomb (B+L) recently announced it has received 510(k) clearance from the U.S. FDA for Vitesse™ — reportedly the first and only hypersonic, 100 percent open port vitrectomy system.

Vitesse features a single lumen design with a fixed open-port for consistent flow. It reportedly creates a highly-localized tissue liquification zone to liquefy the vitreous at the edge of the port before aspiration. According to B+L, vitreous removal is currently performed with a guillotine style vitrectomy cutter. This pneumatically driven vitrectomy cutter employs a needle-inside-a-needle design to perform a guillotine cut of the vitreous which is then aspirated.

This new technology will reportedly be featured exclusively on the new Stellaris Elite™ Vision Enhancement System.

Click here to read the full press release.

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Source: Bausch + Lomb

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