510(k) Report

510(k) · Cleared

Cleared

Rmo Plasma Curing Light

K024374510(k) TraditionalCleared Mar 10, 200369-day reviewClass II21 CFR 872.6070

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

Lokki Lasers Medicaux · EBZ Activator, Ultraviolet, For Polymerization

Cleared on Mar 10, 2003 after a 69-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 2 later devices descend from it.

Decided
Mar 10, 2003
Review
69 days
Class
Class II
Product code
EBZ
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared2008: 1 descendant cleared200020052010201520202025
  1. This deviceK024374 Rmo Plasma Curing LightLokki Lasers Medicaux · 2003
  2. Descendant · cites it directly · 1 of its ownK033795 Plasmacure BxeEele Laboratories, LLC · 2003
  3. Descendant · 2 generations on · 0 of its ownK081287 Sapphire Plasma Arc Dental Curing LightDen-Mat Holdings, LLC · 2008

Most influential descendants

Showing 2 of 2 · See all
  • K033795Plasmacure BxeEele Laboratories, LLC · 2003 · cites it directly1descendant
  • K081287Sapphire Plasma Arc Dental Curing LightDen-Mat Holdings, LLC · 2008 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K024374Rmo Plasma Curing LightLokki Lasers Medicaux2003—
+1K033795Plasmacure BxeEele Laboratories, LLC2003—
+2K081287Sapphire Plasma Arc Dental Curing LightDen-Mat Holdings, LLC2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
200810
FIG. 1 — Lineage of K024374, 2003–2008Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EBZ? 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 EBZ device

  1. #1 K253131 Curing Light (M-Cure 6)score 12.7 · 5 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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K033795Plasmacure BxeEele Laboratories, LLC20031

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?

  • Of its descendants, K033795 (Eele Laboratories, LLC, 2003) has gone furthest, with 1 descendant of its own.

How does its category compare?

All EBZ devices

EBZ Activator, Ultraviolet, For Polymerization: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EBZ

4in 2025

2007: 102008: 52009: 42010: 12011: 32012: 12013: 32014: 32015: 42016: 42017: 82018: 22019: 52020: 52021: 12022: 52023: 32024: 12025: 42026 (partial year): 1
2007high 10 (2007) · low 1 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBZ

105in 2025

2007: 47 days median2008: 75 days median2009: 69 days median2011: 137 days median2013: 171 days median2014: 289 days median2015: 252 days median2016: 251 days median2017: 158 days median2019: 145 days median2020: 164 days median2022: 144 days median2023: 255 days median2025: 105 days median
2007high 289 (2014) · low 47 (2007)2026

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

Recalls per year · EBZ

1in 2022

2012: 12018: 12022: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · EBZ

1in 2025

2007: 12008: 72009: 52010: 52011: 182012: 202013: 272014: 312015: 82016: 32017: 52018: 32020: 22021: 42022: 52023: 72024: 32025: 1
2007high 31 (2014) · low 0 (2019)2025

MAUDE reports naming product code EBZ, 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
2007104701
200857507
200946905
20101—05
20113137018
20121—120
20133171027
20143289031
2015425208
2016425103
2017815805
20182—13
2019514500
2020516402
20211—04
2022514415
2023325507
20241—03
2025410501
20261—0—

What is it indicated for?

The RMO Plasma Curing Light is a source of illumination for curing dental restorative materials and is a source of illumination for tooth whitening activities performed in dentistry.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K024374: Rmo Plasma Curing Light.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K024374

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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