G. Rodenstock Instrumente GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
G. Rodenstock Instrumente GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
G. Rodenstock Instrumente GmbH has 3 FDA 510(k) cleared medical devices. Based in Munchen 70, West Germany, DE.
Historical record: 3 cleared submissions from 1986 to 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by G. Rodenstock Instrumente GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - G. Rodenstock Instrumente GmbH
3 devices