Corneagen, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Corneagen, Inc. has 1 FDA 510(k) cleared medical devices. Based in Winston-Salem, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Corneagen, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by K.Hodai Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Corneagen, Inc.
1 devices