- Milestone strengthens the company’s leadership in advanced IOL innovation
- FINEVISION HP, with millions of implantations worldwide, will now be available to U.S. patients
- Proprietary design features anchor the launch of BVI’s expanded U.S. IOL portfolio
WALTHAM, Mass., Oct. 14, 2025 — BVI, a global leader in ophthalmic device innovation, today announced that the U.S. Food and Drug Administration (FDA) has approved its FINEVISION HP trifocal intraocular lens (IOL). This milestone reinforces BVI’s leadership in premium IOLs and expands advanced vision solutions for U.S. patients. Read More







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