510(k) Report

510(k) · Cleared

Cleared

Opal Band Cement

K111696510(k) TraditionalCleared Sep 7, 201182-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

Ultradent Products, Inc. · DYH Adhesive, Bracket And Tooth Conditioner, Resin

Cleared on Sep 7, 2011 as substantially equivalent to K950514 (3M Unitek, 1995) after an 82-day review. Its family tree reaches back 1 generation to 1995.

Decided
Sep 7, 2011
Review
82 days
Class
Class II
Product code
DYH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K950514 (1995). No later device cites it as a predicate yet.

K950514 · Tri-Cure Glass Ionomer Orthodontic Band Cement · 3M Unitek · 19951995200020052010
  1. Root · 1 generation backK950514 Tri-Cure Glass Ionomer Orthodontic Band Cement3M Unitek · 1995
  2. This deviceK111696 Opal Band CementUltradent Products, Inc. · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K950514Tri-Cure Glass Ionomer Orthodontic Band Cement3M Unitek1995—
0 (this device)K111696Opal Band CementUltradent Products, Inc.2011—
FIG. 1 — Lineage of K111696, 1995–2011Source: 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 13.8 · 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
*K950514Tri-Cure Glass Ionomer Orthodontic Band Cement
Summary page 1
…ssification: 11 Classification Product Code: DYH Legally Marketed Predicate Devices to Which Equivalence is Claimed- The predicate device is: K950514 CC/3M Tni-Cure Glass lonomer Orthodontic Band Cement also known as " Unitek'Multi-Cure Glass lonomer Band Cement" Opal® Band'" C…
3M Unitek1995—

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?

  • Its one ancestor has no recall.

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. 2011, this device’s year, is highlighted.

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?

Opal® BandTM Cement uses chemical, light polymerization and glass jonomer to cement all types of orthodontic bands to the teeth.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111696: Opal Band Cement.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111696

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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