Tri-Star Ophthalmic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tri-Star Ophthalmic - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tri-Star Ophthalmic has 2 FDA 510(k) cleared medical devices. Based in Liberty, US.
Historical record: 2 cleared submissions from 1991 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Tri-Star Ophthalmic Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tri-Star Ophthalmic
2 devices