510(k) Report

510(k) · Cleared

Cleared

Clear Bravo

K083473510(k) TraditionalCleared Jan 22, 200959-day reviewClass II21 CFR 872.3765

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

Denali R&D Corporation · EBC Sealant, Pit And Fissure, And Conditioner

Cleared on Jan 22, 2009 after a 59-day review. The FDA summary names its predicate without a number.

Decided
Jan 22, 2009
Review
59 days
Class
Class II
Product code
EBC
Recalls
None
Predicates
0

The FDA summary names its predicate without a number.

FIG. 1 — Lineage of K083473Source: FDA 510(k) database · 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 EBC? 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 EBC device

  1. #1 K243254 Parkell Pit and Fissure Sealantscore 12.8 · 1 generation · 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? (3)

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
*—CosmeSeal Pit and Fissure Sealant
Named without a submission number
—
*—UltraSeal XT Pit and Fissure Sealant and Flowable Composite Kit
Named without a submission number
—
*—Delton Clear Pit and Fissure Sealant Kit
Named without a submission number
—

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.

How does its category compare?

All EBC devices

EBC Sealant, Pit And Fissure, And Conditioner: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · EBC

1in 2025

2007: 12008: 12009: 22010: 52011: 32012: 12013: 12014: 12015: 12016: 12017: 22018: 12019: 22023: 22025: 12026 (partial year): 1
2007high 5 (2010) · low 0 (2020)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBC

80in 2011

2010: 115 days median2011: 80 days median
2007high 115 (2010) · low 80 (2011)2026

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

Recalls per year · EBC

2in 2016

2015: 12016: 2
2007high 2 (2016) · low 0 (2007)2026

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

Adverse event reports per year · EBC

6in 2025

2007: 32008: 12009: 12011: 52013: 112020: 12022: 12023: 22024: 12025: 6
2007high 11 (2013) · low 0 (2010)2025

MAUDE reports naming product code EBC, 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—03
20081—01
20092—01
2010511500
201138005
20121—00
20131—011
20141—00
20151—10
20161—20
20172—00
20181—00
20192—00
20200—01
20210—00
20220—01
20232—02
20240—01
20251—06
20261—0—

What is it indicated for?

Clear Bravo is a clear, light-cured pit and fissure sealant and sealer for application to the surfaces of teeth, sealing of composite margins and temporary restorations Clear Bravo is available in either fluoride and non-fluoride releasing formulas

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K083473: Clear Bravo.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K083473

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026