Medical Device Manufacturer · KR , Seoul

Nu Eyne Co., Ltd.

5 submissions · 5 cleared · Since 2019
5
Total
5
Cleared
0
Denied

Nu Eyne Co., Ltd. — FDA 510(k) Submissions

Nu Eyne Co., Ltd. has submitted 5 FDA 510(k) premarket notifications since 2019, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Electrical, Transcutaneous, For Migraine, Transcutaneous Nerve Stimulator For Adhd . Use the specialty filter in the sidebar to narrow results.

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All5 Neurology 5