Lasag AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lasag AG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lasag AG has 2 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 2 cleared submissions from 1989 to 1990. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Lasag AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lasag AG
2 devices