Omnivision AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Omnivision AG - FDA 510(k) Cleared Devices
Recent clearances: MaxiTears Contacts PF
1
Total
1
Cleared
0
Denied
Omnivision AG has 1 FDA 510(k) cleared medical devices. Based in Neuhausen Am Rheinfall, CH.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Omnivision AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Omnivision AG
1 devices