510(k) · Cleared
ClearedClick-IT
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Tp Orthodontics, Inc. · NJM Bracket, Ceramic, Orthodontic
Cleared on May 13, 2011 as substantially equivalent to K081415 (Ormco Corp., 2008) and 2 other predicates after an 11-day review. Its family tree reaches back 3 generations to 1985. 1 later device descends from it.
- Decided
- May 13, 2011
- Review
- 11 days
- Class
- Class II
- Product code
- NJM
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 3 generations to K852179 (1985). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 3 generations backK852179 Ceramic Orthodonit ApplianceGac Intl., Inc. · 1985
- 2 generations backK042178 Orthodontic Ceramic BracketsDentsply Intl. · 2004
- 1 generation backK060837 IN-Ovation CDentsply International · 2006
- This deviceK111234 Click-ITTp Orthodontics, Inc. · 2011
- Descendant · cites it directly · 0 of its ownK160957 CDB Self Ligating Bracket 8FCdb Corporation · 2016
Most influential descendants
Showing 1 of 1 · See all- K160957CDB Self Ligating Bracket 8FCdb Corporation · 2016 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K852179 | Ceramic Orthodonit Appliance | Gac Intl., Inc. | 1985 | — |
| −2 | K042178 | Orthodontic Ceramic Brackets | Dentsply Intl. | 2004 | — |
| −1 | K060837 | IN-Ovation C | Dentsply International | 2006 | — |
| 0 (this device) | K111234 | Click-IT | Tp Orthodontics, Inc. | 2011 | — |
| +1 | K160957 | CDB Self Ligating Bracket 8F | Cdb Corporation | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
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 K222764 LightForce Orthodontic Systemscore 8.5 · 6 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K081415 | Damon 4CLEARSummary page 1…ket Orthodontic Classification Name: Bracket, Ceramic, Orthodontic 21 CFR 872.5470 Device for Which Substantial Equivalence is Claimed Ormco Corporation, Damon 4Clear (K081415) Dentsply International, In-Ovation C (K060837) 3M Unitek Corporation, Clarity Modified Ceramic Bracket (K062305) Device Descri… | 2008 |
| * | K060837 | IN-Ovation CSummary page 1…eramic, Orthodontic 21 CFR 872.5470 Device for Which Substantial Equivalence is Claimed Ormco Corporation, Damon 4Clear (K081415) Dentsply International, In-Ovation C (K060837) 3M Unitek Corporation, Clarity Modified Ceramic Bracket (K062305) Device Description The Click-It ceramic self-ligating bracke… | 2006 |
| * | K062305 | Clarity Modified Ceramic BracketsSummary page 1…Equivalence is Claimed Ormco Corporation, Damon 4Clear (K081415) Dentsply International, In-Ovation C (K060837) 3M Unitek Corporation, Clarity Modified Ceramic Bracket (K062305) Device Description The Click-It ceramic self-ligating bracket is intended to be used in an orthodontic treatment with the aim… | 2006 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K160957 | CDB Self Ligating Bracket 8F | 2016 | 0 |
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 5.1 years on median.
- None of the 5 ancestors has a recall.
- Of its descendants, K160957 (Cdb Corporation, 2016) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K081415.
How does its category compare?
All NJM devicesNJM Bracket, Ceramic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · NJM
5in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · NJM
1in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NJM
1in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NJM
1in 2025
MAUDE reports naming product code NJM, 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 | 1 | — | 0 | 0 |
| 2008 | 4 | 134 | 0 | 0 |
| 2009 | 4 | 61 | 0 | 1 |
| 2010 | 1 | — | 0 | 2 |
| 2011 | 4 | 122 | 0 | 1 |
| 2012 | 6 | 90 | 0 | 1 |
| 2013 | 3 | 123 | 1 | 6 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 3 | 234 | 0 | 0 |
| 2016 | 3 | 176 | 0 | 2 |
| 2017 | 3 | 183 | 0 | 2 |
| 2018 | 4 | 76 | 0 | 2 |
| 2019 | 6 | 200 | 0 | 0 |
| 2020 | 2 | — | 0 | 1 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 2 | — | 0 | 0 |
| 2023 | 5 | 1 | 0 | 1 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Click-it ceramic self-ligating bracket is intended to be used in an orthodontic treatment with the aim of moving teeth.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K111234 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111234: Click-IT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111234
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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