510(k) Report

510(k) · Cleared

Cleared

Acceledent

K110661510(k) TraditionalCleared Nov 17, 2011254-day reviewClass II21 CFR 872.5470

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

Orthoaccel Technologies, Inc. · OYH Orthodontic Vibratory Accessory

Cleared on Nov 17, 2011 as substantially equivalent to K924975 (Myofunctional Research Corp. Pty., Ltd., 1993) after a 254-day review. Its family tree reaches back 1 generation to 1993. 6 later devices descend from it.

Decided
Nov 17, 2011
Review
254 days
Class
Class II
Product code
OYH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K924975 (1993). 6 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2013: 1 descendant cleared2015: 1 descendant cleared2016: 1 descendant cleared2023: 1 descendant cleared2019: 1 descendant cleared2017: 1 descendant clearedK924975 · The Orthotrainer · Myofunctional Research Corp. Pty., Ltd. · 19931990200020102020
Descendants, by generation 1 generation forward: 2 descendants2 generations forward: 2 descendants3 generations forward: 2 descendants K924975 · The Orthotrainer · Myofunctional Research Corp. Pty., Ltd. · 19930
  1. Root · 1 generation backK924975 The OrthotrainerMyofunctional Research Corp. Pty., Ltd. · 1993
  2. This deviceK110661 AcceledentOrthoaccel Technologies, Inc. · 2011
  3. Descendant · cites it directly · 5 of its ownK130643 Acceledent AuraOrthoaccel Technologies, Inc. · 2013
  4. Descendant · cites it directly · 4 of its ownK143120 OrthoPulseBiolux Research, Ltd. · 2015
  5. Descendant · 2 generations on · 2 of its ownK153048 AcceleDent AuraOrthoaccel Technologies, Inc. · 2016
  6. Descendant · 2 generations on · 0 of its ownK230905 OrthoPulse 2.0E (OPi2E-100)Biolux Technology GmbH · 2023
  7. Descendant · 3 generations on · 0 of its ownK183018 VPro5Propel Orthodontics, LLC · 2019

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2013: 12015: 12016: 12017: 12019: 12023: 1
2013high 1 (2013) · low 0 (2014)2026

Most influential descendants

Showing 5 of 6 · See all
  • K130643Acceledent AuraOrthoaccel Technologies, Inc. · 2013 · cites it directly5descendants
  • K143120OrthoPulseBiolux Research, Ltd. · 2015 · cites it directly4descendants
  • K153048AcceleDent AuraOrthoaccel Technologies, Inc. · 2016 · 2 generations on2descendants
  • K230905OrthoPulse 2.0E (OPi2E-100)Biolux Technology GmbH · 2023 · 2 generations on0descendants
  • K183018VPro5Propel Orthodontics, LLC · 2019 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K924975The OrthotrainerMyofunctional Research Corp. Pty., Ltd.1993—
0 (this device)K110661AcceledentOrthoaccel Technologies, Inc.2011—
+1K130643Acceledent AuraOrthoaccel Technologies, Inc.2013—
+1K143120OrthoPulseBiolux Research, Ltd.2015—
+2K153048AcceleDent AuraOrthoaccel Technologies, Inc.2016—
+2K230905OrthoPulse 2.0E (OPi2E-100)Biolux Technology GmbH2023—
+3K183018VPro5Propel Orthodontics, LLC2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201510
201610
201710
201910
202310
FIG. 1 — Lineage of K110661, 1993–2023Source: 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 OYH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (1)

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
*K924975The Orthotrainer
Summary page 1
…Class 11 Panel: Dental Product code: 0TH Regulation number: 872.5470 Predicate device: The Orthotrainer, K924975 Device Description: The AcceleDent TM System is an orthodontic accessory for the treatment of tooth malocclusion. AcceleDentTM…
Myofunctional Research Corp. Pty., Ltd.1993—

What descends from it? (6)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K130643Acceledent AuraOrthoaccel Technologies, Inc.20135
K143120OrthoPulseBiolux Research, Ltd.20154

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?

  • Its one ancestor has no recall.
  • Of its descendants, K130643 (Orthoaccel Technologies, Inc., 2013) has gone furthest, with 5 descendants of its own.

How does its category compare?

All OYH devices

OYH Orthodontic Vibratory Accessory: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · OYH

1in 2019

2011: 12013: 12016: 12017: 12019: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OYH

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

Recalls per year · OYH

No recall names OYH since 2007.

Adverse event reports per year · OYH

2in 2025

2021: 12022: 12024: 12025: 2
2007high 2 (2025) · low 0 (2007)2025

MAUDE reports naming product code OYH, 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—00
20080—00
20090—00
20100—00
20111—00
20120—00
20131—00
20140—00
20150—00
20161—00
20171—00
20180—00
20191—00
20200—00
20210—01
20220—01
20230—00
20240—01
20250—02
20260—0—

What is it indicated for?

AcceleDent is an orthodontic accessory intended for use during orthodontic treatment. It is used in conjunction with orthodontic appliances such as braces and helps facilitate minor anterior tooth movement.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110661: Acceledent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110661

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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