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.
510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.
2 devices