Keta Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keta Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Keta Corp. has 3 FDA 510(k) cleared medical devices. Based in Danvers, US.
Historical record: 3 cleared submissions from 1984 to 1986. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Keta Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Keta Corp.
3 devices