510(k) Report

510(k) · Cleared

Cleared

VENUS Bracket, ROSE Bracket

K201410510(k) TraditionalCleared Mar 12, 2021288-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

Gni Co., Ltd. · NJM Bracket, Ceramic, Orthodontic

Cleared on Mar 12, 2021 as substantially equivalent to K182672 (Gni Co., Ltd., 2019) after a 288-day review. Its family tree reaches back 3 generations to 2007.

Decided
Mar 12, 2021
Review
288 days
Class
Class II
Product code
NJM
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K073045 (2007). No later device cites it as a predicate yet.

  1. Root · 3 generations backK073045 Sapphire Ceramic BracketOrtho Technology, Inc. · 2007
  2. 2 generations backK150141 Orthodontics BracketSpeed Dental Co., Ltd. · 2015
  3. 1 generation backK182672 ROSA BracketGni Co., Ltd. · 2019
  4. This deviceK201410 VENUS Bracket, ROSE BracketGni Co., Ltd. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K073045Sapphire Ceramic BracketOrtho Technology, Inc.2007—
−2K150141Orthodontics BracketSpeed Dental Co., Ltd.2015—
−1K182672ROSA BracketGni Co., Ltd.2019—
0 (this device)K201410VENUS Bracket, ROSE BracketGni Co., Ltd.2021—
FIG. 1 — Lineage of K201410, 2007–2021Source: 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 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
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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
*K182672ROSA Bracket
Summary page 5
…orthodontic treatment has been completed. The devices are intended to be single use only Primary Predicate Device: Primary Manufacturer: GNI Co., LTD 510(k) Number: K182672 Trade Name: ROSA Bracket Common Name: Orthodontic Ceramic Brackets Regulation Name: Orthodontic Plastic Bracket Regulation Number…
Gni Co., Ltd.2019—

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 14 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
  • None of the 3 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. 2021, 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?

This device is intended for the orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed. The devices are intended to be single use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201410: VENUS Bracket, ROSE Bracket.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201410

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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