510(k) Report

510(k) · Cleared

Cleared

Sonendo Endotherapy System

K130025510(k) TraditionalCleared Jun 11, 2013159-day reviewClass II21 CFR 872.4850

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

Sonendo, Inc. · ELC Scaler, Ultrasonic

Cleared on Jun 11, 2013 as substantially equivalent to K093000 (E.M.S Electro Medical Systems S.A, 2010) and 1 other predicate after a 159-day review. Its family tree reaches back 1 generation to 2009. 3 later devices descend from it.

Decided
Jun 11, 2013
Review
159 days
Class
Class II
Product code
ELC
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K081268 (2009). 2 ancestors in all. 3 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2014: 1 descendant cleared2015: 1 descendant cleared2024: 1 descendant clearedK081268 · Sonic Air MM1500 + (Mid), Model 50400014 · Micro-Mega Societe Anonyme · 200920052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 1 descendant K081268 · Sonic Air MM1500 + (Mid), Model 50400014 · Micro-Mega Societe Anonyme · 20090
  1. Root · 1 generation backK081268 Sonic Air MM1500 + (Mid), Model 50400014Micro-Mega Societe Anonyme · 2009
  2. This deviceK130025 Sonendo Endotherapy SystemSonendo, Inc. · 2013
  3. Descendant · cites it directly · 2 of its ownK133752 Sonendo Omniclean Endotherpay System Console, Sonendo Omniclean…Sonendo, Inc. · 2014
  4. Descendant · 2 generations on · 1 of its ownK143448 Sonendo GentleWave SystemSonendo, Inc. · 2015
  5. Descendant · 3 generations on · 0 of its ownK233844 OdneCleanOdne AG · 2024

Most influential descendants

Showing 3 of 3 · See all
  • K133752Sonendo Omniclean Endotherpay System Console, Sonendo Omniclean Molar Procedure KitSonendo, Inc. · 2014 · cites it directly2descendants
  • K143448Sonendo GentleWave SystemSonendo, Inc. · 2015 · 2 generations on1descendant
  • K233844OdneCleanOdne AG · 2024 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K081268Sonic Air MM1500 + (Mid), Model 50400014Micro-Mega Societe Anonyme2009—
0 (this device)K130025Sonendo Endotherapy SystemSonendo, Inc.2013—
+1K133752Sonendo Omniclean Endotherpay System Console, Sonendo Omniclean Molar…Sonendo, Inc.2014—
+2K143448Sonendo GentleWave SystemSonendo, Inc.2015—
+3K233844OdneCleanOdne AG2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
202410
FIG. 1 — Lineage of K130025, 2009–2024Source: 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), 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 ELC? 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 ELC device

  1. #1 K260773 Varios Combi Pro2score 12.5 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K093000Ems Piezon Master 700
Summary page 1
…d Irrigation System gi:f; :FICATION ‘ Ultrasonic Scaler DEVICE Class 2, per 21 CFR 872.4850 CLASSIFICATION: PrODUCT CODE ELC PREDICATE DEVICES: EMS Piezon Master 700 (K093000) Sonic Air MM 1500+.(MID) (K081268) Substantially Equivalent To: The Sonendo Endotherapy System is substantially equivalent in…
E.M.S Electro Medical Systems S.A2010—
*K081268Sonic Air MM1500 + (Mid), Model 50400014
Summary page 1
…‘ Ultrasonic Scaler DEVICE Class 2, per 21 CFR 872.4850 CLASSIFICATION: PrODUCT CODE ELC PREDICATE DEVICES: EMS Piezon Master 700 (K093000) Sonic Air MM 1500+.(MID) (K081268) Substantially Equivalent To: The Sonendo Endotherapy System is substantially equivalent in intended use, principal of operatio…
Micro-Mega Societe Anonyme2009—

Also cleared against K093000: 6 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K133752Sonendo Omniclean Endotherpay System Console, Sonendo Omniclean Molar Procedure KitSonendo, Inc.20142

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?

  • None of the 2 ancestors has a recall.
  • Of its descendants, K133752 (Sonendo, Inc., 2014) has gone furthest, with 2 descendants of its own.
  • 6 other devices also cite its predicate K093000.

How does its category compare?

All ELC devices

ELC Scaler, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · ELC

2in 2025

2007: 62008: 42009: 42010: 42011: 32012: 12013: 132014: 62015: 52016: 32017: 22018: 12019: 42020: 12021: 32022: 22023: 52024: 42025: 22026 (partial year): 2
2007high 13 (2013) · low 1 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ELC

104in 2024

2007: 92 days median2008: 216 days median2009: 121 days median2010: 201 days median2011: 122 days median2013: 174 days median2014: 193 days median2015: 150 days median2016: 88 days median2019: 192 days median2021: 196 days median2023: 258 days median2024: 104 days median
2007high 258 (2023) · low 88 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ELC

2in 2022

2022: 2
2007high 2 (2022) · low 0 (2007)2026

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

Adverse event reports per year · ELC

284in 2025

2007: 122008: 582009: 1082010: 792011: 52012: 32013: 62014: 372015: 1352016: 1692017: 3562018: 2892019: 3022020: 1642021: 1662022: 1652023: 2102024: 2192025: 284
2007high 356 (2017) · low 3 (2012)2025

MAUDE reports naming product code ELC, 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
2007692012
20084216058
200941210108
20104201079
2011312205
20121—03
20131317406
20146193037
201551500135
20163880169
20172—0356
20181—0289
201941920302
20201—0164
202131960166
20222—2165
202352580210
202441040219
20252—0284
20262—0—

What is it indicated for?

The Sonendo Endotherapy System is intended to prepare, clean and irrigate 1* and 2™ molar teeth indicated for root canal therapy.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K130025: Sonendo Endotherapy System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K130025

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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