510(k) Report

510(k) · Cleared

Cleared

Progressive Orthodontics App

K241153510(k) TraditionalCleared Oct 11, 2024168-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

Progressive Aligners, Inc. · PNN Orthodontic Software

Cleared on Oct 11, 2024 as substantially equivalent to K181112 (Orchestrate 3D, 2018) after a 168-day review. Its family tree reaches back 4 generations to 2009.

Decided
Oct 11, 2024
Review
168 days
Class
Class II
Product code
PNN
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K082207 (2009). No later device cites it as a predicate yet.

  1. Root · 4 generations backK082207 Orthocad IQCadent, Inc. · 2009
  2. 3 generations backK152086 3Shape Ortho System3Shape A/S · 2016
  3. 2 generations backK171634 Ortho System3Shape A/S · 2018
  4. 1 generation backK181112 Orchestrate 3DOrchestrate 3D · 2018 · Recalled
  5. This deviceK241153 Progressive Orthodontics AppProgressive Aligners, Inc. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K082207Orthocad IQCadent, Inc.2009—
−3K1520863Shape Ortho System3Shape A/S2016—
−2K171634Ortho System3Shape A/S2018—
−1K181112Orchestrate 3DOrchestrate 3D20181
0 (this device)K241153Progressive Orthodontics AppProgressive Aligners, Inc.2024—
FIG. 1 — Lineage of K241153, 2009–2024Source: 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 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. #1 K262196 Invisalign Systemscore 14.5 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K181112Orchestrate 3D
Summary page 5
…Medical Device, Class II Regulation Number: 21 CFR 872.5470 Predicate Device: Orchestrate 3D Orthodontic Software (K181112) Device Description: The Progressive Orthodontics App is an orthodontic appliance design and treatment simulation software. T…
Orchestrate 3D20181

Also cleared against K181112: 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 15 years and passes through 4 companies; a new generation was cleared every 5.9 years on median.
  • 1 of the 4 ancestors has a recall of any class.
  • 1 other device also cites its predicate K181112.

How does its category compare?

All PNN devices

PNN Orthodontic Software: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · PNN

2in 2025

2016: 12017: 22018: 52019: 22020: 72021: 42022: 12023: 32024: 42025: 22026 (partial year): 6
2007high 7 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PNN

177in 2024

2018: 229 days median2020: 221 days median2021: 58 days median2023: 90 days median2024: 177 days median2026 (partial year): 98 days median
2007high 229 (2018) · low 58 (2021)2026

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

Recalls per year · PNN

1in 2022

2021: 12022: 1
2007high 1 (2021) · low 0 (2007)2026

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

Adverse event reports per year · PNN

1in 2024

2024: 1
2007high 1 (2024) · low 0 (2007)2025

MAUDE reports naming product code PNN, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20161—00
20172—00
2018522900
20192—00
2020722100
202145810
20221—10
202339000
2024417701
20252—00
20266980—

What is it indicated for?

The Progressive Orthodontics App is indicated for use as a front-end software tool for management of orthodontic models, systematic inspection, detailed analysis, treatment simulation and virtual appliance design options, which may be used for sequential aligner trays or retainers. These applications are based on 3D scans of the patient's dentition before the start of an orthodontic treatment. It can also be applied during the treatment to inspect and…

Read the full statement (134 words)

The Progressive Orthodontics App is indicated for use as a front-end software tool for management of orthodontic models, systematic inspection, detailed analysis, treatment simulation and virtual appliance design options, which may be used for sequential aligner trays or retainers. These applications are based on 3D scans of the patient's dentition before the start of an orthodontic treatment. It can also be applied during the treatment to inspect and analyze the progress of the treatment. It can be used at the end of the treatment to evaluate if the outcome is consistent with the planned/desired treatment objectives.

The use of the Progressive Orthodontics App requires the user to have the necessary training and domain knowledge in the practice of orthodontics, as well as to have received a dedicated training in the use of the software.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K241153: Progressive Orthodontics App.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241153

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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