510(k) Report

510(k) · Cleared

Cleared

AD-Hear

K915794510(k) TraditionalCleared Mar 12, 199279-day reviewClass I21 CFR 874.3300

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

Hearing Components, Inc. · ESD Hearing Aid, Air-Conduction, Prescription

Cleared on Mar 12, 1992 after a 79-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Mar 12, 1992
Review
79 days
Class
Class I
Product code
ESD
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1990200020102020
  1. This deviceK915794 AD-HearHearing Components, Inc. · 1992
  2. Descendant · cites it directly · 0 of its ownK984518 Sonic Innovations Completely-in-the-Canal DSP Hearing Aid with Soft…Sonic Innovations, Inc. · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K984518Sonic Innovations Completely-in-the-Canal DSP Hearing Aid with Soft ShellSonic Innovations, Inc. · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K915794AD-HearHearing Components, Inc.1992—
+1K984518Sonic Innovations Completely-in-the-Canal DSP Hearing Aid with Soft ShellSonic Innovations, Inc.1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K915794, 1992–1999Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in ESD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new ESD device

  1. #1 K232999 Lyric4 Hearing Aidscore 8.4 · 5 generations · no Class I recall
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K984518Sonic Innovations Completely-in-the-Canal DSP Hearing Aid with Soft ShellSonic Innovations, Inc.19990

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K984518 (Sonic Innovations, Inc., 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All ESD devices

ESD Hearing Aid, Air-Conduction, Prescription: FDA decisions, review times, recalls and adverse event reports over 20 years.

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—
Cite this page

510(k) Report. “K915794: AD-Hear.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K915794

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026