Optina Diagnostics, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Optina Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Optina-4C (MHRC-C1N), Optina-4C (MHRC-C1N)
2
Total
2
Cleared
0
Denied
Optina Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Latest FDA clearance: Sep 2025. Active since 2023. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Optina Diagnostics, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Optina Diagnostics, Inc.
2 devices