Medical Device Manufacturer · CA , Quebec City

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

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

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.

FDA 510(k) cleared devices by Zilia, Inc.

1 devices
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