510(k) Report

510(k) · Cleared

Cleared

Demi Pro

K253461510(k) TraditionalCleared Oct 14, 20257-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

Meta Systems Co., Ltd. · EBZ Activator, Ultraviolet, For Polymerization

Cleared on Oct 14, 2025 as substantially equivalent to K220471 (Ultradent Products, Inc., 2022) and 1 other predicate after a 7-day review. Its family tree reaches back 8 generations to 2001.

Decided
Oct 14, 2025
Review
7 days
Class
Class II
Product code
EBZ
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K003995 (2001). 18 ancestors in all, the oldest K003383 (2001). No later device cites it as a predicate yet.

  1. Root · 8 generations backK003995 Speculite/OralliteTrylon Corp. · 2001
  2. 7 generations backK060920 VelscopeLed Medical Diagnostics, Inc. · 2006
  3. 6 generations backK070523 Modification to: VelscopeLed Dental, Inc. · 2007
  4. 5 generations backK082603 Trimira Ocs 3000Remicalm, LLC · 2008
  5. 4 generations backK090135 Trimira Identafi 3000Remicalm, LLC · 2009
  6. 3 generations backK101140 Dentlight Oral Exam Light KitDentlight, Inc. · 2010
  7. 2 generations backK210550 VALO Grand Corded and Accessory LensesUltradent Products, Inc. · 2021
  8. 1 generation backK220471 VALO X, VALO X Accessory LensesUltradent Products, Inc. · 2022
  9. This deviceK253461 Demi ProMeta Systems Co., Ltd. · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K003995Speculite/OralliteTrylon Corp.2001—
−7K060920VelscopeLed Medical Diagnostics, Inc.2006—
−6K070523Modification to: VelscopeLed Dental, Inc.2007—
−5K082603Trimira Ocs 3000Remicalm, LLC2008—
−4K090135Trimira Identafi 3000Remicalm, LLC2009—
−3K101140Dentlight Oral Exam Light KitDentlight, Inc.2010—
−2K210550VALO Grand Corded and Accessory LensesUltradent Products, Inc.2021—
−1K220471VALO X, VALO X Accessory LensesUltradent Products, Inc.2022—
0 (this device)K253461Demi ProMeta Systems Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200120
200410
200510
200820
200910
201510
201710
201910
FIG. 1 — Lineage of K253461, 2001–2025Source: 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 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? (2)

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
*K220471VALO X, VALO X Accessory Lenses
Summary page 5
…Product Code(s) EBZ Legally Marketed Predicate Devices Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K220471 VALO X EBZ K170529 Delight Ortho…
Ultradent Products, Inc.2022—
*K170529Delight, Delight ortho, B&Lite S
Summary page 5
…cate # Predicate Trade Name (Primary Predicate is listed first) Product Code K220471 VALO X EBZ K170529 Delight Ortho EBZ Device Description Summary General information: The…
Dentall Co., Ltd.2017—

Also cleared against K220471: 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 24 years and passes through 7 companies; a new generation was cleared every 1.7 years on median.
  • None of the 18 ancestors has a recall.
  • 1 other device also cites its predicate K220471.

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. 2025, this device’s year, is highlighted.

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 Demi Pro is an LED visible light curing unit intended for polymerization of light-cured materials by dental professionals. It is also intended to provide illumination to aid in visualization during oral procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K253461: Demi Pro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K253461

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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