510(k) Report

510(k) · Cleared

Cleared

Straight T Clear Dental Aligner

K201450510(k) TraditionalCleared Sep 10, 2020101-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

Straight T, Inc. · NXC Aligner, Sequential

Cleared on Sep 10, 2020 as substantially equivalent to K173784 (Smylio, Inc., 2018) after a 101-day review. Its family tree reaches back 1 generation to 2018. 1 later device descends from it.

Decided
Sep 10, 2020
Review
101 days
Class
Class II
Product code
NXC
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K173784 (2018). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2022: 1 descendant clearedReference device: K152086 · 3Shape Ortho System · 3Shape A/S · 2016K173784 · Smylic Invisible Clear Aligners · Smylio, Inc. · 2018201620182020202220242026
Descendants, by generation 1 generation forward: 1 descendant K173784 · Smylic Invisible Clear Aligners · Smylio, Inc. · 20180
  1. Root · 1 generation backK173784 Smylic Invisible Clear AlignersSmylio, Inc. · 2018
  2. This deviceK201450 Straight T Clear Dental AlignerStraight T, Inc. · 2020
  3. Descendant · cites it directly · 0 of its ownK213026 Clear AlignerShenzhen Meiming Dentistry Technology Co., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K213026Clear AlignerShenzhen Meiming Dentistry Technology Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K173784Smylic Invisible Clear AlignersSmylio, Inc.2018—
0 (this device)K201450Straight T Clear Dental AlignerStraight T, Inc.2020—
+1K213026Clear AlignerShenzhen Meiming Dentistry Technology Co., Ltd.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K201450, 2018–2022Source: 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 NXC? 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 NXC device

  1. #1 K220287 Invisalign Systemscore 20.3 · 5 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
*K173784Smylic Invisible Clear Aligners
Summary page 4
…#301, Surprise AZ 85374 (623)474-384 Minh Trinh May 20, 2020 Straight T Clear Dental Aligner Aligners, Sequential Orthodontic Plastic Bracket 21 CFR 872.5470 NXC 2 K173784, Smylio Invisible Clear Aligner The Straight T Clear Dental Aligners indicated for use in the alignment of permanent teeth (i.e.…
Smylio, Inc.2018—
†K1804913Shape Software—
†K1520863Shape Ortho System3Shape A/S2016—

Also cleared against K173784: 4 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K213026Clear AlignerShenzhen Meiming Dentistry Technology Co., Ltd.20220

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?

  • Its one ancestor has no recall.
  • Of its descendants, K213026 (Shenzhen Meiming Dentistry Technology Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K173784.

How does its category compare?

All NXC devices

NXC Aligner, Sequential: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NXC

11in 2025

2007: 12008: 22009: 22010: 12012: 22013: 42015: 22016: 12017: 32018: 112019: 162020: 162021: 202022: 192023: 132024: 142025: 112026 (partial year): 5
2007high 20 (2021) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NXC

61in 2025

2013: 124 days median2017: 85 days median2018: 116 days median2019: 182 days median2020: 230 days median2021: 97 days median2022: 137 days median2023: 152 days median2024: 105 days median2025: 61 days median2026 (partial year): 127 days median
2007high 230 (2020) · low 61 (2025)2026

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

Recalls per year · NXC

2in 2024

2024: 2
2007high 2 (2024) · low 0 (2007)2026

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

Adverse event reports per year · NXC

4,523in 2025

2007: 12008: 52009: 22010: 112011: 592012: 242013: 282014: 272015: 432016: 412017: 472018: 672019: 1272020: 1752021: 9292022: 6052023: 4332024: 8,9912025: 4,523
2007high 8,991 (2024) · low 1 (2007)2025

MAUDE reports naming product code NXC, 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—01
20082—05
20092—02
20101—011
20110—059
20122—024
20134124028
20140—027
20152—043
20161—041
2017385047
201811116067
2019161820127
2020162300175
202120970929
2022191370605
2023131520433
20241410528,991
2025116104,523
202651270—

What is it indicated for?

The Straight T Clear Dental Aligners indicated for use in the alignment of permanent teeth (i.e. all second molars) through orthodontic treatment of misalignment and malocclusion.

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. “K201450: Straight T Clear Dental Aligner.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201450

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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