510(k) Report

510(k) · Cleared

Cleared

Braces on Demand Bracket

K201940510(k) TraditionalCleared Dec 3, 2020143-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

Braces on Demand, Inc. · DYW Bracket, Plastic, Orthodontic

Cleared on Dec 3, 2020 as substantially equivalent to K140807 (Ortho Specialties, 2014) and 1 other predicate after a 143-day review. Its family tree reaches back 6 generations to 1985.

Decided
Dec 3, 2020
Review
143 days
Class
Class II
Product code
DYW
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K852179 (1985). 12 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 6 generations backK852179 Ceramic Orthodonit ApplianceGac Intl., Inc. · 1985
  2. 5 generations backK042178 Orthodontic Ceramic BracketsDentsply Intl. · 2004
  3. 4 generations backK082974 Mystique MB Ceramic BracketsDentsply Interntional · 2008
  4. 3 generations backK090454 Allure MB Ceramic BracketsDentsply Interntional · 2009
  5. 2 generations backK092030 Elation MB Metal Reinforced Plastic BracketDentsply Interntional · 2009
  6. 1 generation backK140807 Composite Orthodontic BracketsOrtho Specialties · 2014
  7. This deviceK201940 Braces on Demand BracketBraces on Demand, Inc. · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K852179Ceramic Orthodonit ApplianceGac Intl., Inc.1985—
−5K042178Orthodontic Ceramic BracketsDentsply Intl.2004—
−4K082974Mystique MB Ceramic BracketsDentsply Interntional2008—
−3K090454Allure MB Ceramic BracketsDentsply Interntional2009—
−2K092030Elation MB Metal Reinforced Plastic BracketDentsply Interntional2009—
−1K140807Composite Orthodontic BracketsOrtho Specialties2014—
0 (this device)K201940Braces on Demand BracketBraces on Demand, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200910
201610
201820
FIG. 1 — Lineage of K201940, 1985–2020Source: 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 DYW? 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 DYW device

  1. #1 K252760 Carriere® Motion Pro® Clear Bite Correctorscore 10.4 · 1 generation · no Class I recall
  2. #2 Held for the reportin the report
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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
*K140807Composite Orthodontic Brackets
Summary page 4
…21 CFR 872.5470 Product Code DYW PNN Regulatory Class 2 2 Predicate Name K140807, Composite Brackets, K180941, 3Shape Ortho Ortho Specialties, Inc. System™; 3Shape A/S R…
Ortho Specialties2014—
*K180941Ortho System
Summary page 4
…duct Code DYW PNN Regulatory Class 2 2 Predicate Name K140807, Composite Brackets, K180941, 3Shape Ortho Ortho Specialties, Inc. System™; 3Shape A/S Reference Device K172398, Dentca D…
3Shape A/S2018—
†K172398DENTCA DENTURE TeethDentca, Inc.2017—

Also cleared against K140807: 1 other device →

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 35 years and passes through 5 companies; a new generation was cleared every 5.3 years on median.
  • None of the 12 ancestors has a recall.
  • 1 other device also cites its predicate K140807.

How does its category compare?

All DYW devices

DYW Bracket, Plastic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · DYW

2in 2025

2007: 22008: 12009: 22010: 12011: 12012: 12013: 22014: 12016: 32018: 22020: 12025: 2
2007high 3 (2016) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DYW

372in 2016

2016: 372 days median
2007high 372 (2016)2026

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

Recalls per year · DYW

2in 2011

2011: 2
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · DYW

1in 2017

2007: 22014: 42015: 42017: 1
2007high 4 (2014) · low 0 (2008)2025

MAUDE reports naming product code DYW, 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
20072—02
20081—00
20092—00
20101—00
20111—20
20121—00
20132—00
20141—04
20150—04
2016337200
20170—01
20182—00
20190—00
20201—00
20210—00
20220—00
20230—00
20240—00
20252—00
20260—0—

What is it indicated for?

The Braces on Demand Bracket is intended for use as a clear, plastic bracket system to provide orthodontic movement of

natural teeth.

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. “K201940: Braces on Demand Bracket.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201940

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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