Oertli Instrumente AG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Oertli Instrumente AG has 2 FDA 510(k) cleared medical devices. Based in Berneck, CH.
Latest FDA clearance: Jun 2024. Active since 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oertli Instrumente AG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Oertli Instrumente AG
2 devices