510(k) Report

510(k) · Cleared

Cleared

ID Light Cure System

K250804510(k) TraditionalCleared Jun 4, 202579-day reviewClass II21 CFR 872.3310

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

Id Korea Co., Ltd. · EBD Coating, Filling Material, Resin

Cleared on Jun 4, 2025 as substantially equivalent to K133836 (GC America, Inc., 2014) after a 79-day review. Its family tree reaches back 2 generations to 2005.

Decided
Jun 4, 2025
Review
79 days
Class
Class II
Product code
EBD
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K052462 (2005). No later device cites it as a predicate yet.

K052462 · G-COAT · GC America, Inc. · 2005K133836 · Optiglaze Color · GC America, Inc. · 201420052010201520202025
  1. Root · 2 generations backK052462 G-COATGC America, Inc. · 2005
  2. 1 generation backK133836 Optiglaze ColorGC America, Inc. · 2014
  3. This deviceK250804 ID Light Cure SystemId Korea Co., Ltd. · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K052462G-COATGC America, Inc.2005—
−1K133836Optiglaze ColorGC America, Inc.2014—
0 (this device)K250804ID Light Cure SystemId Korea Co., Ltd.2025—
FIG. 1 — Lineage of K250804, 2005–2025Source: 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 EBD? 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 EBD device

  1. #1 K254091 Glossy Coat (15ML)score 11.4 · 2 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
*K133836Optiglaze Color
Summary page 5
…21 CFR 807.92國 Pred icate # Pred i cate Trade Name (Pr i mary Pred icate i s li sted fi rst) Product Code I K133836 ] I OPTIGLAZE COLOR ] I• EBO Device Descr…
GC America, Inc.2014—

Also cleared against K133836: 3 other devices →

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 20 years and passes through 2 companies; a new generation was cleared every 11.2 years on median.
  • None of the 2 ancestors has a recall.
  • 3 other devices also cite its predicate K133836.

How does its category compare?

All EBD devices

EBD Coating, Filling Material, Resin: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · EBD

1in 2025

2007: 12008: 32009: 12013: 12014: 12017: 12018: 12021: 12023: 12024: 12025: 12026 (partial year): 1
2007high 3 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBD

76in 2008

2008: 76 days median
2007high 76 (2008)2026

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

Recalls per year · EBD

No recall names EBD since 2007.

Adverse event reports per year · EBD

5in 2023

2008: 22009: 22017: 12021: 12023: 5
2007high 5 (2023) · low 0 (2007)2025

MAUDE reports naming product code EBD, 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
200837602
20091—02
20100—00
20110—00
20120—00
20131—00
20141—00
20150—00
20160—00
20171—01
20181—00
20190—00
20200—00
20211—01
20220—00
20231—05
20241—00
20251—00
20261—0—

What is it indicated for?

Crown, Bridges, Veneer, Onlay & Inlay, Denture, partial denture, Orthodontic appliance, Splints.

- Characterization of direct & indirect composite restorations, acrylic denture base and artificial acrylic teeth.

- For obtaining surface smoothness and wear resistance of restorations made of composite resin, acrylic denture base and artificial acrylic teeth.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K250804: ID Light Cure System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K250804

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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