Single-patient use
Designed for one patient and not intended for reuse.
Akoya offers product samples, a brief staff demonstration, and a flexible one-site evaluation framework for organizations reviewing patient-comfort tools in selected needle-based workflows.
Akoya Eye Shield is an optional visual barrier. Each healthcare organization and clinical team determines whether, where, and how it is appropriate to evaluate or use the product.
Designed for one patient and not intended for reuse.
Supplied nonsterile. Site-specific handling and disposal requirements remain under organizational review.
The current marketed product is represented by Akoya as latex-free.
Currently available by quote in quantities aligned with organizational needs.
Potential settings have not all been clinically evaluated with Akoya Eye Shield. They are presented for review by the participating organization's clinical, compliance, and procurement teams.
Optional use for patients who prefer not to see peripheral IV access activity.
Potential review during selected oncology and infusion access workflows.
Potential review during phlebotomy or other vascular-access encounters.
Potential review during selected injections or image-guided procedures.
A 30-day, one-site starting framework can be adjusted to the organization's patient volume, review process, and operational needs.
Akoya supplies product samples, current available documentation, and a brief product demonstration focused on fit and positioning.
The organization selects the site, patients, workflow, scope, and duration under its own clinical, compliance, privacy, and procurement requirements.
The organization determines whether any further review, flexible volume pricing, or paid institutional rollout discussion is appropriate.
Akoya can provide a simple draft staff and patient feedback template. The participating organization decides whether feedback is collected and governs all applicable clinical, privacy, compliance, and research requirements. Akoya does not need patient-identifying information for a basic product discussion.
Workflow fit, staff observations, ease of positioning, product handling, and descriptive patient experience. A limited product evaluation is not presented as proof of clinical effectiveness.
A concise, organization-neutral product sheet covering the design, current product facts, evaluation pathway, early feedback limitations, and contacts.
Download the product overviewPublic record for U.S. Patent No. 12,629,282 B1, issued May 19, 2026, naming Drew Richard Zaun and Thomas Raymond Goetz as inventors.
View the public patent recordDrew is the primary contact for healthcare organizations and brings Tom into product-development questions when helpful. Our response target is within two business days.
Founder & Chief Sales & Marketing Officer
Product samples, institutional pricing, evaluation discussions, and purchasing.
Contact DrewCo-Owner & Head of Product
Tom supports product design, fit, documentation, and evaluation questions behind the scenes. Drew coordinates the conversation.