Zilia, Inc. - FDA 510(k) Cleared Devices

Zilia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Quebec City, CA.

Last cleared in 2023. Active since 2023. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Zilia, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Ultra Life Science Solutions, Inc. as regulatory consultant.