510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221698Substantially Equivalent

Eargo 5 , Eargo 6

Eargo Inc, San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221698 is the FDA 510(k) clearance record for Eargo 5 , Eargo 6, a class II device, cleared for Eargo, Inc. on under FDA product code QUH (Self-Fitting Air-Conduction Hearing Aid, Over The Counter). FDA's definition for product code QUH reads: "A self-fitting air-conduction hearing aid is a wearable sound amplifying device that is intended to compensate for impaired hearing and incorporates technology, including software, that allows users to program their hearing aids. This...". FDA records list one 510(k) clearance for Eargo, Inc. As of , FDA records show no recalls naming K221698.

Clearance record

Decision date
Received
(191 days to decision)
Product code
QUH Self-Fitting Air-Conduction Hearing Aid, Over The Counter
Regulation
21 CFR 874.3325
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Eargo, Inc. 2665 N. First St., Suite 300, San Jose CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QUH

Trailing 12 months
1 clearance under product code QUH in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QUH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260