Class Class II

Lenire Tinnitus Treatment Device (DEN210033)

DEN210033 2023-03-06 Direct
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Description

Lenire Tinnitus Treatment Device by Neuromod Devices Limited, an FDA 510(k) cleared ear, nose, throat device.

Regulatory Information

Device ClassClass Class II
510(k) NumberDEN210033
Clearance Date2023-03-06
Clearance TypeDirect
Product CodeQVN
Regulation Number874.3410

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