510(k) · Cleared
ClearedCelebrace Software
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Celebrace · PNN Orthodontic Software
Cleared on Dec 29, 2025 as substantially equivalent to K233625 (Ray Co., Ltd., 2024) and 2 other predicates after a 90-day review. Its family tree reaches back 6 generations to 2009.
- Decided
- Dec 29, 2025
- Review
- 90 days
- Class
- Class II
- Product code
- PNN
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 6 generations to K082207 (2009). 12 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK082207 Orthocad IQCadent, Inc. · 2009
- 5 generations backK152086 3Shape Ortho System3Shape A/S · 2016
- 4 generations backK171634 Ortho System3Shape A/S · 2018
- 3 generations backK191720 BRUIS Software SuiteMechanodontics, Inc. · 2020
- 2 generations backK212828 BRIUS Planner SoftwareBrius Technologies, Inc. · 2021
- 1 generation backK232429 Titan Dental DesignClearadvance, LLC · 2023
- This deviceK253343 Celebrace SoftwareCelebrace · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K082207 | Orthocad IQ | Cadent, Inc. | 2009 | — |
| −5 | K152086 | 3Shape Ortho System | 3Shape A/S | 2016 | — |
| −4 | K171634 | Ortho System | 3Shape A/S | 2018 | — |
| −3 | K191720 | BRUIS Software Suite | Mechanodontics, Inc. | 2020 | — |
| −2 | K212828 | BRIUS Planner Software | Brius Technologies, Inc. | 2021 | — |
| −1 | K232429 | Titan Dental Design | Clearadvance, LLC | 2023 | — |
| 0 (this device) | K253343 | Celebrace Software | Celebrace | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2018 | 3 | 0 |
| 2021 | 1 | 0 |
| 2024 | 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 PNN? 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 PNN device
- #1 K262196 Invisalign Systemscore 14.5 · 9 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 |
|---|---|---|---|
| * | K233625 | Raydent SWSummary page 6…Celebrace Software, has been shown to be appropriate for its indications for use and is as safe and as effective as the legally marketed Predicate Device, Raydent SW (1<233625). There are no substantial differences between the indications for use, technological features, or performance testing of the Sub… | 2024 |
| * | K232429 | Titan Dental Design | 2023 |
| * | K203442 | Inbrace Orthodontic System | 2021 |
| † | K233925 | Relu Creator | 2024 |
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 16 years and passes through 6 companies; a new generation was cleared every 2.2 years on median.
- None of the 12 ancestors has a recall.
- 1 other device also cites its predicate K233625.
How does its category compare?
All PNN devicesPNN Orthodontic Software: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · PNN
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · PNN
177in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PNN
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · PNN
1in 2024
MAUDE reports naming product code PNN, 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 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 5 | 229 | 0 | 0 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 7 | 221 | 0 | 0 |
| 2021 | 4 | 58 | 1 | 0 |
| 2022 | 1 | — | 1 | 0 |
| 2023 | 3 | 90 | 0 | 0 |
| 2024 | 4 | 177 | 0 | 1 |
| 2025 | 2 | — | 0 | 0 |
| 2026 | 6 | 98 | 0 | — |
What is it indicated for?
Celebrace software is a software designed to assist dental professionals in planning patient treatment and designing treatment devices. The software performs simulations based on patient images, allowing reference to treatment plans, and is used as a tool to design treatment devices based on 3D mesh data. Treatment devices include orthodontic devices (orthodontic wires, orthodontic brackets and bonding trays).
To use Celebrace Software, users must have the necessary education and domain knowledge in orthodontic practice and receive dedicated training in the use of the software.
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/K253343 · printed Nov 4, 2026
Cite this page
510(k) Report. “K253343: Celebrace Software.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K253343
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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