Zilia, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Zilia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Zilia Ocular FC (ZIL-10002)
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.
510(k) submissions have been managed by Ultra Life Science Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zilia, Inc.
1 devices