510(k) Report

510(k) · Cleared

Cleared

DT-703

K221233510(k) TraditionalCleared Jun 27, 202259-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

Ecotron Co., Ltd. · EHD Unit, X-Ray, Extraoral With Timer

Cleared on Jun 27, 2022 as substantially equivalent to K173319 (Aribex, 2017) after a 59-day review. Its family tree reaches back 5 generations to 2000. 1 later device descends from it.

Decided
Jun 27, 2022
Review
59 days
Class
Class II
Product code
EHD
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K000061 (2000). 1 later device descends from it, 1 citing it directly.

  1. Root · 5 generations backK000061 Minxray HF70D High Frequency Portable Dental X-Ray UnitMinxray, Inc. · 2000
  2. 4 generations backK021378 Portable HDX Intraoral X-RayDentalez Group · 2002 · Recalled
  3. 3 generations backK051795 Nomad Dental X-Ray SystemAribex, Inc. · 2005
  4. 2 generations backK081664 Nomad Pro X-Ray SystemAribex, Inc. · 2008 · Recalled
  5. 1 generation backK173319 KaVo NOMAD Pro 2 Handheld X-ray SystemAribex · 2017
  6. This deviceK221233 DT-703Ecotron Co., Ltd. · 2022
  7. Descendant · cites it directly · 0 of its ownK260367 Portable Dental X-ray System Model PDX novaPDX Co., Ltd. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K000061Minxray HF70D High Frequency Portable Dental X-Ray UnitMinxray, Inc.2000—
−4K021378Portable HDX Intraoral X-RayDentalez Group20021
−3K051795Nomad Dental X-Ray SystemAribex, Inc.2005—
−2K081664Nomad Pro X-Ray SystemAribex, Inc.20082
−1K173319KaVo NOMAD Pro 2 Handheld X-ray SystemAribex2017—
0 (this device)K221233DT-703Ecotron Co., Ltd.2022—
+1K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K221233, 2000–2026Source: 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 EHD? 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 EHD device

  1. #1 K260795 Hand-held Dental X-ray System (HyperLight-M)score 14.1 · 8 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? (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
*K173319KaVo NOMAD Pro 2 Handheld X-ray System
Summary page 4
…: II Product Code: EHD 3. Predicate Device: Proprietary Name: KaVo NOMAD Pro 2 Handheld X-ray System (K173319) Manufacturer Name: Aribex Common Name: Handheld X-ray System Classification Na…
Aribex2017—

Also cleared against K173319: 7 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
K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.20260

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 22 years and passes through 5 companies; a new generation was cleared every 3.1 years on median.
  • 2 of the 5 ancestors have a recall of any class.
  • Of its descendants, K260367 (PDX Co., Ltd., 2026) has gone furthest, with 0 descendants of its own.
  • 7 other devices also cite its predicate K173319.

How does its category compare?

All EHD devices

EHD Unit, X-Ray, Extraoral With Timer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · EHD

1in 2025

2007: 12008: 52009: 42010: 42011: 32012: 22013: 42014: 32015: 12016: 22017: 42018: 52019: 42020: 22021: 12022: 82023: 82024: 72025: 12026 (partial year): 6
2007high 8 (2022) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EHD

58in 2024

2008: 49 days median2009: 92 days median2010: 268 days median2011: 102 days median2013: 216 days median2014: 107 days median2017: 28 days median2018: 30 days median2019: 173 days median2022: 58 days median2023: 147 days median2024: 58 days median2026 (partial year): 128 days median
2007high 268 (2010) · low 28 (2017)2026

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

Recalls per year · EHD

1in 2017

2010: 32011: 32014: 12016: 12017: 1
2007high 3 (2010) · low 0 (2007)2026

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

Adverse event reports per year · EHD

6in 2024

2007: 52008: 62009: 382010: 472011: 262012: 222013: 212014: 202015: 1102016: 632017: 662018: 212019: 212020: 42021: 42022: 42023: 22024: 6
2007high 110 (2015) · low 0 (2025)2025

MAUDE reports naming product code EHD, 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—05
200854906
2009492038
20104268347
20113102326
20122—022
20134216021
20143107120
20151—0110
20162—163
2017428166
2018530021
20194173021
20202—04
20211—04
202285804
2023814702
202475806
20251—00
202661280—

What is it indicated for?

The DT-703 is a portable dental X-ray system that captures radiographic images for dental diagnosis using intraoral imaging sensors. Only trained and qualified dental practitioner or radiologist shall use DT-703 to diagnose and treat diseases related to the teeth, jaws, and/or other oral structures in adults and children.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K221233: DT-703.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K221233

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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