510(k) Report

510(k) · Cleared

Cleared

LightForce Orthodontic System

K232827510(k) TraditionalCleared Sep 14, 20231-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

Lightforce Orthodontics · NJM Bracket, Ceramic, Orthodontic

Cleared on Sep 14, 2023 as substantially equivalent to K222764 (Lightforce Orthodontics, 2022) after a 1-day review. Its family tree reaches back 7 generations to 1985.

Decided
Sep 14, 2023
Review
1 day
Class
Class II
Product code
NJM
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K852179 (1985). 14 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK852179 Ceramic Orthodonit ApplianceGac Intl., Inc. · 1985
  2. 6 generations backK042178 Orthodontic Ceramic BracketsDentsply Intl. · 2004
  3. 5 generations backK082974 Mystique MB Ceramic BracketsDentsply Interntional · 2008
  4. 4 generations backK102803 Clarity Advanced Ceramic Brackets3M Unitek Corporation · 2011
  5. 3 generations backK160615 Orthodontic Ceramic Brackets 1.1Tomy, Inc. · 2016
  6. 2 generations backK181271 Signature Orthodontic SystemSignature Orthodontics · 2018
  7. 1 generation backK222764 LightForce Orthodontic SystemLightforce Orthodontics · 2022
  8. This deviceK232827 LightForce Orthodontic SystemLightforce Orthodontics · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K852179Ceramic Orthodonit ApplianceGac Intl., Inc.1985—
−6K042178Orthodontic Ceramic BracketsDentsply Intl.2004—
−5K082974Mystique MB Ceramic BracketsDentsply Interntional2008—
−4K102803Clarity Advanced Ceramic Brackets3M Unitek Corporation2011—
−3K160615Orthodontic Ceramic Brackets 1.1Tomy, Inc.2016—
−2K181271Signature Orthodontic SystemSignature Orthodontics2018—
−1K222764LightForce Orthodontic SystemLightforce Orthodontics2022—
0 (this device)K232827LightForce Orthodontic SystemLightforce Orthodontics2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199510
200620
200910
201210
201310
FIG. 1 — Lineage of K232827, 1985–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 NJM? 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 NJM device

  1. #1 K222764 LightForce Orthodontic Systemscore 8.5 · 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? (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
*K222764LightForce Orthodontic System
Summary page 4
…duct Code: NJM, PNN Regulatory Class: II Predicate Devices: Primary Predicate: LightForce Orthodontic System (K222764) Reference Predicate: Dentsply International IN-OVATION C brackets (K060837) Device Description: The LightForce Orthodo…
Lightforce Orthodontics2022—
†K060837IN-Ovation CDentsply International2006—
†K160957CDB Self Ligating Bracket 8FCdb Corporation2016—

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 38 years and passes through 7 companies; a new generation was cleared every 4.2 years on median.
  • None of the 14 ancestors has a recall.

How does its category compare?

All NJM devices

NJM Bracket, Ceramic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · NJM

5in 2023

2007: 12008: 42009: 42010: 12011: 42012: 62013: 32014: 12015: 32016: 32017: 32018: 42019: 62020: 22021: 12022: 22023: 5
2007high 6 (2012) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NJM

1in 2023

2008: 134 days median2009: 61 days median2011: 122 days median2012: 90 days median2013: 123 days median2015: 234 days median2016: 176 days median2017: 183 days median2018: 76 days median2019: 200 days median2023: 1 days median
2007high 234 (2015) · low 1 (2023)2026

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

Recalls per year · NJM

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · NJM

1in 2025

2009: 12010: 22011: 12012: 12013: 62016: 22017: 22018: 22020: 12023: 12024: 22025: 1
2007high 6 (2013) · low 0 (2007)2025

MAUDE reports naming product code NJM, 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
20071—00
2008413400
200946101
20101—02
2011412201
201269001
2013312316
20141—00
2015323400
2016317602
2017318302
201847602
2019620000
20202—01
20211—00
20222—00
20235101
20240—02
20250—01
20260—0—

What is it indicated for?

The LightForce Orthodontic System is a treatment planning software and orthodontic appliance system used to correct malocclusions in orthodontic patients using patient-matched orthodontic appliances.

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. “K232827: LightForce Orthodontic System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K232827

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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