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

Altris, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.

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

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.