Ocusciences, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ocusciences, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ocusciences, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Healthcare Technologies Consultants, LLC as regulatory consultant.
1 devices