510(k) Report

510(k) · Cleared

Cleared

Intraoral Belsensor Gold

K102456510(k) TraditionalCleared Dec 15, 2011475-day reviewClass II21 CFR 872.1800

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

Takara Belmont USA, Inc. · MUH System, X-Ray, Extraoral Source, Digital

Cleared on Dec 15, 2011 as substantially equivalent to K090458 (Dexis, LLC, 2009) after a 475-day review. Its family tree reaches back 4 generations to 1994. 1 later device descends from it.

Decided
Dec 15, 2011
Review
475 days
Class
Class II
Product code
MUH
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K933455 (1994). 7 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2004: 1 other ancestor2002: 1 other ancestor2012: 1 descendant clearedK933455 · Computed Oral Radiology System · Schick Technologies, Inc. · 1994K022953 · Modification to Computed Oral Radiology System · Schick Technologies, Inc. · 2002K072134 · Schick Computed Oral Radiology System · Schick Technologies, Inc. · 2007K090458 · Dexis Sensor · Dexis, LLC · 20091990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors 1 generation forward: 1 descendant K090458 · Dexis Sensor · Dexis, LLC · 2009K072134 · Schick Computed Oral Radiology System · Schick Technologies, Inc. · 2007K022953 · Modification to Computed Oral Radiology System · Schick Technologies, Inc. · 2002K933455 · Computed Oral Radiology System · Schick Technologies, Inc. · 19940
  1. Root · 4 generations backK933455 Computed Oral Radiology SystemSchick Technologies, Inc. · 1994
  2. 3 generations backK022953 Modification to Computed Oral Radiology SystemSchick Technologies, Inc. · 2002
  3. 2 generations backK072134 Schick Computed Oral Radiology SystemSchick Technologies, Inc. · 2007
  4. 1 generation backK090458 Dexis SensorDexis, LLC · 2009
  5. This deviceK102456 Intraoral Belsensor GoldTakara Belmont USA, Inc. · 2011
  6. Descendant · cites it directly · 0 of its ownK123419 Eva Select Digital Dental Imaging SystemAfp Imaging Corp. · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K123419Eva Select Digital Dental Imaging SystemAfp Imaging Corp. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K933455Computed Oral Radiology SystemSchick Technologies, Inc.1994—
−3K022953Modification to Computed Oral Radiology SystemSchick Technologies, Inc.2002—
−2K072134Schick Computed Oral Radiology SystemSchick Technologies, Inc.2007—
−1K090458Dexis SensorDexis, LLC2009—
0 (this device)K102456Intraoral Belsensor GoldTakara Belmont USA, Inc.2011—
+1K123419Eva Select Digital Dental Imaging SystemAfp Imaging Corp.2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200410
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K102456, 1994–2012Source: 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 MUH? 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 MUH device

  1. #1 K242778 X Sensor (Model: IOS-A15IF, HDI-15DGF)score 16.0 · 7 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
*K090458Dexis Sensor
Summary page 1
…872.1800 Classification Code: MUH Substantially Equivalent/Predicate Devices (21 CFR 807.92(a)(3)) Predicate Device 1: IDExiS Sensor (K090458) Device Description (21 CIFR 807.92(a)(4)) The BelSensor GOLD is an indirect converting x-ray detector that converts incident…
Dexis, LLC2009—

Also cleared against K090458: 6 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K123419Eva Select Digital Dental Imaging SystemAfp Imaging Corp.20120

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 17 years and passes through 3 companies; a new generation was cleared every 5.1 years on median.
  • None of the 7 ancestors has a recall.
  • Of its descendants, K123419 (Afp Imaging Corp., 2012) has gone furthest, with 0 descendants of its own.
  • 6 other devices also cite its predicate K090458.

How does its category compare?

All MUH devices

MUH System, X-Ray, Extraoral Source, Digital: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · MUH

3in 2025

2007: 112008: 82009: 92010: 92011: 102012: 92013: 92014: 82015: 122016: 62017: 92018: 32019: 52020: 52021: 102022: 72023: 112024: 42025: 32026 (partial year): 2
2007high 12 (2015) · low 3 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MUH

159in 2025

2007: 48 days median2008: 64 days median2009: 88 days median2010: 174 days median2011: 89 days median2012: 81 days median2013: 172 days median2014: 168 days median2015: 111 days median2016: 47 days median2017: 84 days median2018: 29 days median2019: 64 days median2020: 36 days median2021: 80 days median2022: 57 days median2023: 57 days median2024: 144 days median2025: 159 days median
2007high 174 (2010) · low 29 (2018)2026

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

Recalls per year · MUH

1in 2015

2008: 12009: 22013: 12014: 12015: 1
2007high 2 (2009) · low 0 (2007)2026

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

Adverse event reports per year · MUH

1in 2025

2009: 122010: 92012: 52013: 12014: 52015: 32016: 12017: 42018: 102019: 62021: 12023: 12025: 1
2007high 12 (2009) · low 0 (2007)2025

MAUDE reports naming product code MUH, 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
2007114800
200886410
2009988212
2010917409
2011108900
201298105
2013917211
2014816815
20151211113
201664701
201798404
2018329010
201956406
202053600
2021108001
202275700
2023115701
2024414400
2025315901
20262—0—

What is it indicated for?

The BelSensor GOLD is a USB-driven digital sensor which is intended to acquire dental intra-oral radiology images. The BelSensor GOLD shall be operated by healthcare professionals, who are educated and competent to perform the acquisition of dental intra-oral radiographs. The BelSensor GOLD can be used either in combination with special positioning devices to facilitate positioning and alignment with the x-ray beam or it may also be positioned by hand with the assistance of a patient.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K102456: Intraoral Belsensor Gold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K102456

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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