510(k) Report

510(k) · Cleared

Cleared

Digital Radiography Cxdi-60G

K081648510(k) TraditionalCleared Jun 24, 200812-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. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Jun 24, 2008 as substantially equivalent to K031447 (Canon, Inc., 2003) after a 12-day review. Its family tree reaches back 4 generations to 1998. 91 later devices descend from it.

Decided
Jun 24, 2008
Review
12 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K981556 (1998). 5 ancestors in all. 91 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2011: 8 descendants cleared2009: 2 descendants cleared2013: 3 descendants cleared2010: 2 descendants cleared2012: 2 descendants cleared2016: 6 descendants cleared2014: 5 descendants cleared2025: 6 descendants cleared2017: 8 descendants cleared2019: 6 descendants cleared2022: 12 descendants cleared2021: 6 descendants cleared2018: 10 descendants cleared2020: 4 descendants cleared2015: 1 descendant cleared2024: 6 descendants cleared2023: 2 descendants cleared2026: 2 descendants clearedK981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 1998K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 20031995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 4 descendants3 generations forward: 8 descendants4 generations forward: 9 descendants5 generations forward: 11 descendants6 generations forward: 17 descendants7 generations forward: 13 descendants8 generations forward: 6 descendants9 generations forward: 8 descendants10 generations forward: 3 descendants11 generations forward: 3 descendants12 generations forward: 3 descendants13 generations forward: 3 descendants K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 2003K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 19980+5+10
  1. Root · 4 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 3 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 2 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 1 generation backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. This deviceK081648 Digital Radiography Cxdi-60GCanon, Inc. · 2008
  6. Descendant · cites it directly · 82 of its ownK091545 Digital Radiography Cxdi-60CCanon, Inc. · 2009
  7. Descendant · 2 generations on · 80 of its ownK102012 Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · Recalled
  8. Descendant · 3 generations on · 54 of its ownK103596 Wireless/Wired FDR D-Evo Flat Panel DetectorFujifilm Medical Systems U.S.A, Inc. · 2011
  9. Descendant · 3 generations on · 52 of its ownK111548 Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600…Fujifilm Medical System U.S.A., Inc. · 2011
  10. Descendant · 4 generations on · 50 of its ownK132509 FDR D-Evo Flat Panel Detector SystemFujifilm Medical Systems U.S.A, Inc. · 2013

Showing 5 of 91 descendants. See all descendants

Descendants cleared per year

2009: 22010: 22011: 82012: 22013: 32014: 52015: 12016: 62017: 82018: 102019: 62020: 42021: 62022: 122023: 22024: 62025: 62026: 2
2009high 12 (2022) · low 1 (2015)2026

Most influential descendants

Showing 5 of 91 · See all
  • K091545Digital Radiography Cxdi-60CCanon, Inc. · 2009 · cites it directly82descendants
  • K102012Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · 2 generations on80descendants
  • K103596Wireless/Wired FDR D-Evo Flat Panel DetectorFujifilm Medical Systems U.S.A, Inc. · 2011 · 3 generations on54descendants
  • K111548Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600 W/DR-ID611SEFujifilm Medical System U.S.A., Inc. · 2011 · 3 generations on52descendants
  • K132509FDR D-Evo Flat Panel Detector SystemFujifilm Medical Systems U.S.A, Inc. · 2013 · 4 generations on50descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−3K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−2K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−1K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
0 (this device)K081648Digital Radiography Cxdi-60GCanon, Inc.2008—
+1K091545Digital Radiography Cxdi-60CCanon, Inc.2009—
+2K102012Digital RadiographyCanon Inc. -Medical Equipment Group20101
+3K103596Wireless/Wired FDR D-Evo Flat Panel DetectorFujifilm Medical Systems U.S.A, Inc.2011—
+3K111548Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600 W/DR-ID611SEFujifilm Medical System U.S.A., Inc.2011—
+4K132509FDR D-Evo Flat Panel Detector SystemFujifilm Medical Systems U.S.A, Inc.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200920
201020
201180
201220
201330
201450
201510
201660
201780
2018100
201960
202040
202160
2022120
202320
202460
202560
202620
FIG. 1 — Lineage of K081648, 1998–2026Source: 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 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? (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
*K031447Canon, Digital Radiography, Model Cxdi-50G
Summary page 1
…be assigned Predicate Device: Manufacturer: Canon Inc. Trade Name: Canon Model Name: CXDI-50G . Classification Name: 90MQB, Solid State X-ray Imager FDA 510(k) #: K031447 Description Of Device: The Canon digital radiography CXDI-60G is a solid state x-ray imagers. The CXDI-60G intercepts x-ray pho…
Canon, Inc.2003—

Also cleared against K031447: 15 other devices →

What descends from it? (91)

See all 91

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K091545Digital Radiography Cxdi-60CCanon, Inc.200982
K083645Radstar Family, Models: Radstar 4343 & Variations5 Star Medical, Inc.20096
K103348Digiview 250Kub Technologies, Inc.20110

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 10 years and passes through 2 companies; a new generation was cleared every 3.1 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K091545 (Canon, Inc., 2009) has gone furthest, with 82 descendants of its own.
  • 15 other devices also cite its predicate K031447.

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. 2008, 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-60G provides digital image capture for conventional film/screen radiographic examinations.

The device is intended to replace radiographic film/screen systems in all general purpose diagnostic procedures.

This device is 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. “K081648: Digital Radiography Cxdi-60G.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K081648

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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