510(k) Report

510(k) · Cleared

Cleared

Digital Radiography

K111682510(k) SpecialCleared Sep 2, 201179-day reviewClass II21 CFR 892.1680

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

Canon Inc. -Medical Equipment Group · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Sep 2, 2011 as substantially equivalent to K103591 (Canon Inc. -Medical Equipment Group, 2011) and 2 other predicates after a 79-day review. Its family tree reaches back 8 generations to 1998. 3 later devices descend from it.

Decided
Sep 2, 2011
Review
79 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
3

Its longest line of descent runs back 8 generations to K981556 (1998). 16 ancestors in all. 3 later devices descend from it, 1 citing it directly.

  1. Root · 8 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 7 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 6 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 5 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 4 generations backK060433 Digital Radiography Cxdi-50CCanon, Inc. · 2006
  6. 3 generations backK091545 Digital Radiography Cxdi-60CCanon, Inc. · 2009
  7. 2 generations backK102012 Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · Recalled
  8. 1 generation backK103591 Digital RadiographyCanon Inc. -Medical Equipment Group · 2011
  9. This deviceK111682 Digital RadiographyCanon Inc. -Medical Equipment Group · 2011
  10. Descendant · cites it directly · 2 of its ownK153312 Scatter Correction for Cxdi SeriesCanon, Inc. · 2016
  11. Descendant · 2 generations on · 1 of its ownK190368 Enhanced Feature Software Pack CXDI SeriesCanon, Inc. · 2019
  12. Descendant · 3 generations on · 0 of its ownK212269 Intelligent NRCanon, Inc. · 2021

Most influential descendants

Showing 3 of 3 · See all
  • K153312Scatter Correction for Cxdi SeriesCanon, Inc. · 2016 · cites it directly2descendants
  • K190368Enhanced Feature Software Pack CXDI SeriesCanon, Inc. · 2019 · 2 generations on1descendant
  • K212269Intelligent NRCanon, Inc. · 2021 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−7K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−6K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−5K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−4K060433Digital Radiography Cxdi-50CCanon, Inc.2006—
−3K091545Digital Radiography Cxdi-60CCanon, Inc.2009—
−2K102012Digital RadiographyCanon Inc. -Medical Equipment Group20101
−1K103591Digital RadiographyCanon Inc. -Medical Equipment Group2011—
0 (this device)K111682Digital RadiographyCanon Inc. -Medical Equipment Group2011—
+1K153312Scatter Correction for Cxdi SeriesCanon, Inc.2016—
+2K190368Enhanced Feature Software Pack CXDI SeriesCanon, Inc.2019—
+3K212269Intelligent NRCanon, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200310
200510
200610
200810
200930

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201910
202110
FIG. 1 — Lineage of K111682, 1998–2021Source: 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 MQB? 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 MQB device

  1. #1 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 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? (3)

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
*K103591Digital Radiography
Summary page 1
…tal Radiography CXDI-501C Classification Name: 90MQB, Solid State X-ray Imager FDA 510¢k) #: To be assigned Predicate Device: Trade Name: Canon FDA 510(k) #/Model Name: K 103591/ Digital Radiography CXDI-401G COMPACT/CXDI-401C COMPACT K091436/ Digital Radiography CXDI-55C K091435/ Digital Radiography CXDI-…
Canon Inc. -Medical Equipment Group2011—
*K091436Digital Radiography, Model Cxdi-55C
Summary page 1
…X-ray Imager FDA 510¢k) #: To be assigned Predicate Device: Trade Name: Canon FDA 510(k) #/Model Name: K 103591/ Digital Radiography CXDI-401G COMPACT/CXDI-401C COMPACT K091436/ Digital Radiography CXDI-55C K091435/ Digital Radiography CXDI-55G Classu':catlon Name: 90MQB, Solid State X-ray Imager Descri…
Canon, Inc.20091
*K091435Digital Radiography Model Cxdi-55G
Summary page 1
…ned Predicate Device: Trade Name: Canon FDA 510(k) #/Model Name: K 103591/ Digital Radiography CXDI-401G COMPACT/CXDI-401C COMPACT K091436/ Digital Radiography CXDI-55C K091435/ Digital Radiography CXDI-55G Classu':catlon Name: 90MQB, Solid State X-ray Imager Description of Device: The Digital Radiograp…
Canon, Inc.20091

Also cleared against K103591: 3 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K153312Scatter Correction for Cxdi SeriesCanon, Inc.20162

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 13 years and passes through 3 companies; a new generation was cleared every 1.2 years on median.
  • 3 of the 16 ancestors have a recall of any class.
  • Of its descendants, K153312 (Canon, Inc., 2016) has gone furthest, with 2 descendants of its own.
  • 3 other devices also cite its predicate K103591.

How does its category compare?

All MQB devices

MQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · MQB

8in 2025

2007: 132008: 82009: 152010: 112011: 242012: 222013: 212014: 322015: 212016: 222017: 312018: 162019: 222020: 192021: 212022: 312023: 102024: 82025: 82026 (partial year): 3
2007high 32 (2014) · low 8 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQB

127in 2025

2007: 22 days median2008: 15 days median2009: 57 days median2010: 116 days median2011: 102 days median2012: 80 days median2013: 105 days median2014: 102 days median2015: 81 days median2016: 92 days median2017: 30 days median2018: 30 days median2019: 30 days median2020: 28 days median2021: 48 days median2022: 48 days median2023: 30 days median2024: 187 days median2025: 127 days median2026 (partial year): 245 days median
2007high 245 (2026) · low 15 (2008)2026

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

Recalls per year · MQB

1in 2025

2007: 152008: 362009: 192010: 142011: 102012: 82013: 62017: 12018: 42019: 12020: 42021: 12025: 12026 (partial year): 1
2007high 36 (2008) · low 0 (2014)2026

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

Adverse event reports per year · MQB

141in 2025

2007: 252008: 302009: 342010: 392011: 1012012: 2672013: 1592014: 292015: 212016: 262017: 202018: 842019: 452020: 92021: 262022: 132023: 512024: 912025: 141
2007high 267 (2012) · low 9 (2020)2025

MAUDE reports naming product code MQB, 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
200713221525
20088153630
200915571934
2010111161439
20112410210101
201222808267
2013211056159
201432102029
20152181021
20162292026
20173130120
20181630484
20192230145
2020192849
20212148126
20223148013
20231030051
20248187091
202581271141
202632451—

What is it indicated for?

DIGITAL RADIOGRAPHY CXDI-501G and CXDI-501C provide digital image capture for conventional film/screen radiographic examinations.

These devices are intended to replace radiographic film/screen systems in all general purpose diagnostic procedures.

These devices are not intended for mammography applications.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K111682: Digital Radiography.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K111682

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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