Oculocare Medical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Oculocare Medical AG - FDA 510(k) Cleared Devices
Recent clearances: Alleye
1
Total
1
Cleared
0
Denied
Oculocare Medical AG has 1 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculocare Medical AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Oculocare Medical AG
1 devices