Earlens Corporation - FDA 510(k) Cleared Devices
3
Total
2
Cleared
1
Denied
Earlens Corporation has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 2 cleared submissions from 2015 to 2019. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Earlens Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Earlens Corporation
3 devices