510(k) Report

510(k) · Cleared

Cleared

Ideal 1 Orthodontic Band Cement

K040375510(k) TraditionalCleared Apr 2, 200445-day reviewClass II21 CFR 872.3750

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Dentsply Intl. · DYH Adhesive, Bracket And Tooth Conditioner, Resin

Cleared on Apr 2, 2004 as substantially equivalent to K033703 (Dentsply Intl., 2004) after a 45-day review. Its family tree reaches back 2 generations to 1994.

Decided
Apr 2, 2004
Review
45 days
Class
Class II
Product code
DYH
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K933766 (1994). No later device cites it as a predicate yet.

  1. Root · 2 generations backK933766 High-Q-BondSilmet U.S.A. Corp. · 1994
  2. 1 generation backK033703 Ideal 1 Orthodontic Bracket AdhesiveDentsply Intl. · 2004
  3. This deviceK040375 Ideal 1 Orthodontic Band CementDentsply Intl. · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K933766High-Q-BondSilmet U.S.A. Corp.1994—
−1K033703Ideal 1 Orthodontic Bracket AdhesiveDentsply Intl.2004—
0 (this device)K040375Ideal 1 Orthodontic Band CementDentsply Intl.2004—
FIG. 1 — Lineage of K040375, 1994–2004Source: 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 DYH? 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 DYH device

  1. #1 K261840 BracePaste Prime Plusscore 13.9 · 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
*K033703Ideal 1 Orthodontic Bracket Adhesive
Summary page 1
…ME: Bracket adhesive and tooth conditioner resin (872.3'750) PR EDICATE DEVICES: Ideal® 1 Orthodontic Bracket Adhesive K033703 DIMVICE DESCRIPTION: The IDEAL® I ORTHODONTIC BAND CEMENT is a light-cure tw )-part system: an orthodontic cement and a primer…
Dentsply Intl.2004—

Also cleared against K033703: 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 10 years and passes through 2 companies; a new generation was cleared every 10.0 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K033703.

How does its category compare?

All DYH devices

DYH Adhesive, Bracket And Tooth Conditioner, Resin: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DYH

1in 2025

2007: 32008: 62009: 32010: 42011: 22012: 32013: 12015: 52016: 22018: 12019: 12020: 32021: 12022: 12023: 22024: 12025: 12026 (partial year): 3
2007high 6 (2008) · low 0 (2014)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DYH

143in 2020

2007: 62 days median2008: 72 days median2009: 77 days median2010: 96 days median2012: 82 days median2015: 135 days median2020: 143 days median2026 (partial year): 87 days median
2007high 143 (2020) · low 62 (2007)2026

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

Recalls per year · DYH

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · DYH

1in 2025

2007: 22008: 12009: 12010: 52011: 12012: 32014: 22015: 22016: 12017: 52025: 1
2007high 5 (2010) · low 0 (2013)2025

MAUDE reports naming product code DYH, 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
200736212
200867201
200937701
201049605
20112—01
201238203
20131—00
20140—02
2015513502
20162—01
20170—05
20181—00
20191—00
2020314300
20211—00
20221—00
20232—00
20241—00
20251—01
20263870—

What is it indicated for?

Bonding of orthodontic bands to natural and artificial tooth surfaces

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040375: Ideal 1 Orthodontic Band Cement.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K040375

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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