Nuheara Limited is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuheara Limited - FDA 510(k) Cleared Devices
Recent clearances: Nuheara IQbuds 2 PRO Hearing Aid
1
Total
1
Cleared
0
Denied
Nuheara Limited has 1 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Nuheara Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Darthur Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Nuheara Limited
1 devices