Haag-Streit AG is one of 5631 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Haag-Streit AG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Haag-Streit AG has 4 FDA 510(k) cleared medical devices. Based in Wadsworth, US.
Historical record: 4 cleared submissions from 1998 to 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Haag-Streit AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Haag-Streit AG
4 devices