Levo Gen 2 Tinnitus Therapy System
K-Number: K260413 · 2026-08-13
Device Summary
Frequently Asked Questions
What is the Levo Gen 2 Tinnitus Therapy System?
Levo Gen 2 Tinnitus Therapy System is a medical device that received FDA 510(k) clearance on 2026-08-13. The listed applicant is Levo Medical Corporation. The 510(k) number is K260413.
When did Levo Gen 2 Tinnitus Therapy System receive FDA 510(k) clearance?
Levo Gen 2 Tinnitus Therapy System received FDA 510(k) clearance on 2026-08-13, under 510(k) number K260413.
Who is the listed applicant for Levo Gen 2 Tinnitus Therapy System?
The FDA 510(k) record lists Levo Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Levo Gen 2 Tinnitus Therapy System?
The FDA product code for Levo Gen 2 Tinnitus Therapy System is KLW.
Related Devices (Code: KLW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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