Resource Center

Technical documentation, clinical support materials, and press assets for OcuTap.

Downloads

Clinical resources

Fact sheet, team bios, and brand assets are shared together as one request. Request permission and we'll add your email with viewing permission, then send you the link.

  • Restricted PDF document

    Fact sheet

    Device specifications and technical performance data.

    Included in the Press kit request

  • Restricted ZIP file

    Team bios

    Headshots and professional bios for the full Visionaire team.

    Included in the Press kit request

  • Restricted ZIP file

    Brand assets

    High-resolution device photography, logos, and brand identity files.

    Included in the Press kit request

Videos and renders

Stay informed on OcuTap’s regulatory progress

OcuTap is pending U.S. Food and Drug Administration (FDA) clearance, anticipated by the end of 2026. Sign up to get updates and we’ll email you when there’s meaningful news to share.

Investigational device. Limited by Federal law to investigational use. FDA 510(k) clearance anticipated by the end of 2026.

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