510(k) Report

510(k) · Cleared

Cleared

Bernhard-Forster GMBH Orthodontic Ceramic Brackets

K090933510(k) TraditionalCleared Jun 5, 200964-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

Forestadent Bernhard Forster GmbH · NJM Bracket, Ceramic, Orthodontic

Cleared on Jun 5, 2009 as substantially equivalent to K060837 (Dentsply International, 2006) after a 64-day review. Its family tree reaches back 3 generations to 1985. 2 later devices descend from it.

Decided
Jun 5, 2009
Review
64 days
Class
Class II
Product code
NJM
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K852179 (1985). 2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2014: 1 descendant cleared2012: 1 descendant clearedK852179 · Ceramic Orthodonit Appliance · Gac Intl., Inc. · 1985K042178 · Orthodontic Ceramic Brackets · Dentsply Intl. · 2004K060837 · IN-Ovation C · Dentsply International · 20061990200020102020
  1. Root · 3 generations backK852179 Ceramic Orthodonit ApplianceGac Intl., Inc. · 1985
  2. 2 generations backK042178 Orthodontic Ceramic BracketsDentsply Intl. · 2004
  3. 1 generation backK060837 IN-Ovation CDentsply International · 2006
  4. This deviceK090933 Bernhard-Forster GMBH Orthodontic Ceramic BracketsForestadent Bernhard Forster GmbH · 2009
  5. Descendant · cites it directly · 0 of its ownK141104 Truklear BracketAjw Technology Consultants, Inc. · 2014
  6. Descendant · cites it directly · 0 of its ownK120471 Mach Brackets Bright BracketsWorld Bio Tech Co., Ltd. · 2012

Most influential descendants

Showing 2 of 2 · See all
  • K141104Truklear BracketAjw Technology Consultants, Inc. · 2014 · cites it directly0descendants
  • K120471Mach Brackets Bright BracketsWorld Bio Tech Co., Ltd. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K852179Ceramic Orthodonit ApplianceGac Intl., Inc.1985—
−2K042178Orthodontic Ceramic BracketsDentsply Intl.2004—
−1K060837IN-Ovation CDentsply International2006—
0 (this device)K090933Bernhard-Forster GMBH Orthodontic Ceramic BracketsForestadent Bernhard Forster GmbH2009—
+1K141104Truklear BracketAjw Technology Consultants, Inc.2014—
+1K120471Mach Brackets Bright BracketsWorld Bio Tech Co., Ltd.2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201410
FIG. 1 — Lineage of K090933, 1985–2014Source: 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
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
*K060837IN-Ovation C
Summary page 1
…acket CFR 872.5470; NJM classification CFR 872.5470, NJM Applicant Dentsply International Bernhard For:;i.er GrnbH 51 0(k) - Number (1(060837) This submissin Material A1203 ALSO3 Intended use The innov…
Dentsply International2006—

Also cleared against K060837: 8 other devices →

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K141104Truklear BracketAjw Technology Consultants, Inc.20140
K120471Mach Brackets Bright BracketsWorld Bio Tech Co., Ltd.20120

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 24 years and passes through 4 companies; a new generation was cleared every 3.2 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K141104 (Ajw Technology Consultants, Inc., 2014) has gone furthest, with 0 descendants of its own.
  • 8 other devices also cite its predicate K060837.

How does its category compare?

All NJM devices

NJM Bracket, Ceramic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, 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?

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

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090933: Bernhard-Forster GMBH Orthodontic Ceramic Brackets.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K090933

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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