510(k) · Cleared
ClearedVPro5
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Propel Orthodontics, LLC · OYH Orthodontic Vibratory Accessory
Cleared on Nov 1, 2019 as substantially equivalent to K153048 (Orthoaccel Technologies, Inc., 2016) after a 366-day review. Its family tree reaches back 5 generations to 1993.
- Decided
- Nov 1, 2019
- Review
- 366 days
- Class
- Class II
- Product code
- OYH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K924975 (1993). No later device cites it as a predicate yet.
- Root · 5 generations backK924975 The OrthotrainerMyofunctional Research Corp. Pty., Ltd. · 1993
- 4 generations backK110661 AcceledentOrthoaccel Technologies, Inc. · 2011
- 3 generations backK130643 Acceledent AuraOrthoaccel Technologies, Inc. · 2013
- 2 generations backK143120 OrthoPulseBiolux Research, Ltd. · 2015
- 1 generation backK153048 AcceleDent AuraOrthoaccel Technologies, Inc. · 2016
- This deviceK183018 VPro5Propel Orthodontics, LLC · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K924975 | The Orthotrainer | Myofunctional Research Corp. Pty., Ltd. | 1993 | — |
| −4 | K110661 | Acceledent | Orthoaccel Technologies, Inc. | 2011 | — |
| −3 | K130643 | Acceledent Aura | Orthoaccel Technologies, Inc. | 2013 | — |
| −2 | K143120 | OrthoPulse | Biolux Research, Ltd. | 2015 | — |
| −1 | K153048 | AcceleDent Aura | Orthoaccel Technologies, Inc. | 2016 | — |
| 0 (this device) | K183018 | VPro5 | Propel Orthodontics, LLC | 2019 | — |
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
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K153048 | AcceleDent AuraSummary page 4…Orthodontic Vibratory Accessory Product Code: OYH Classification: Class II pursuant to 21 C.F.R. § 872.5470 Predicate Device: AcceleDent® Aura (K153048) Device Description: The VPro5® is a rechargeable, hand-held, powered, high-frequency vibration device… | 2016 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- The line of descent spans 26 years and passes through 4 companies; a new generation was cleared every 2.3 years on median.
- None of the 5 ancestors has a recall.
- 1 other device also cites its predicate K153048.
How does its category compare?
All OYH devicesOYH Orthodontic Vibratory Accessory: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · OYH
1in 2019
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
MAUDE reports naming product code OYH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 0 | — | 0 | 1 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 1 |
| 2025 | 0 | — | 0 | 2 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VPro5 is intended for use by the orthodontic patient during treatment with aligners to facilitate minor anterior tooth movement.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K183018 · printed Nov 6, 2026
Cite this page
510(k) Report. “K183018: VPro5.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K183018
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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