510(k) Report

De Novo · Granted

Granted

Sonu

DEN230045De NovoGranted Dec 4, 2023171-day reviewClass II21 CFR 874.6010

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

Sound Health Systems, Inc. · QZC External Mechanical Stimulator For The Relief Of Congestion

Granted on Dec 4, 2023 as a new device type through De Novo after a 171-day review. 1 later device descends from it.

Decided
Dec 4, 2023
Review
171 days
Class
Class II
Product code
QZC
Recalls
None

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

Descendants, by year cleared 2025: 1 descendant cleared2020202220242026
  1. This deviceDEN230045 SonuSound Health Systems, Inc. · 2023
  2. Descendant · cites it directly · 0 of its ownK242214 SonuSound Health Systems, Inc. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K242214SonuSound Health Systems, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN230045SonuSound Health Systems, Inc.2023—
+1K242214SonuSound Health Systems, Inc.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of DEN230045, 2023–2025Source: 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 De Novo database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in QZC? 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 QZC device

  1. #1 K242214 Sonuscore 9.2 · 1 generation · no Class I recall
Get a 510(k) Report

Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K242214SonuSound Health Systems, Inc.20250

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, K242214 (Sound Health Systems, Inc., 2025) has gone furthest, with 0 descendants of its own.

How does its category compare?

All QZC devices

QZC External Mechanical Stimulator For The Relief Of Congestion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · QZC

1in 2025

2023: 12025: 1
2007high 1 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QZC

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

Recalls per year · QZC

No recall names QZC since 2007.

Adverse event reports per year · QZC

No MAUDE report names QZC since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20231—00
20240—00
20251—00
20260—0—

What is it indicated for?

Sonu is indicated for the relief of moderate to severe nasal congestion due to allergic and non-allergic rhinitis. Sonu is a treatment to be used at home by individuals 22 and older.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “DEN230045: Sonu.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN230045

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026