Surgical Instrument Engineering AG is one of 5654 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Instrument Engineering AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Surgical Instrument Engineering AG has 1 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Surgical Instrument Engineering AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgical Instrument Engineering AG
1 devices