510(k) Report

FDA product code · Ear, nose and throat

Hearing Aid, Air-Conduction, Prescription

ESDClass I21 CFR 874.3300510(k) exempt1,367 decisions since 19764 recalls

FDA lists ESD as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 874.9 applies, such as a new intended use or a different fundamental technology. 1,367 FDA decisions since 1976. 510(k) reviews decided 2021–2025 took a median of 202 days (half between 202 and 202). 4 recalls name this code, 0 of them Class I. The most-cited predicate is K003558, named by 5 later devices.

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, ear, nose and throat panel

Twenty years of ESD at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · ESD

1in 2024

2008: 12013: 12024: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ESD

Too few ESD 510(k)s in any year since 2007 to give a median.

Recalls per year · ESD

2in 2019

2010: 12018: 12019: 2
2007high 2 (2019) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ESD

53in 2025

2007: 132008: 132009: 32010: 12011: 32012: 62013: 372014: 42015: 62016: 72017: 42018: 122019: 92020: 52021: 42022: 42023: 82024: 162025: 53
2007high 53 (2025) · low 1 (2010)2025

MAUDE reports naming product code ESD, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—013
20081—013
20090—03
20100—11
20110—03
20120—06
20131—037
20140—04
20150—06
20160—07
20170—04
20180—112
20190—29
20200—05
20210—04
20220—04
20230—08
20241—016
20250—053
20260—0—
FIG. 1 — ESD by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ESD? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 874.3300.