510(k) Report

510(k) · Cleared

Cleared

Digital Radiography CXDI-Pro, Digital Radiography D1

K222855510(k) SpecialCleared Oct 17, 202226-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 Oct 17, 2022 as substantially equivalent to K221876 (Canon, Inc., 2022) after a 26-day review. Its family tree reaches back 14 generations to 1998.

Decided
Oct 17, 2022
Review
26 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 14 generations to K981556 (1998). 20 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 14 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 10 generations between
  3. 3 generations backK212553 DIGITAL RADIOGRAPHY CXDI-Pro, D1Canon, Inc. · 2021
  4. 2 generations backK220098 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
  5. 1 generation backK221876 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
  6. This deviceK222855 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
Show all 14 generations
  1. Root · 14 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 13 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 12 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 11 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 10 generations backK060433 Digital Radiography Cxdi-50CCanon, Inc. · 2006
  6. 9 generations backK091545 Digital Radiography Cxdi-60CCanon, Inc. · 2009
  7. 8 generations backK102012 Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · Recalled
  8. 7 generations backK103591 Digital RadiographyCanon Inc. -Medical Equipment Group · 2011
  9. 6 generations backK112309 Digital RadiographyCanon Inc. -Medical Equipment Group · 2011
  10. 5 generations backK131106 Digital Radiography Cxdi-701C Wireless, Digital Radiography…Canon, Inc. · 2013
  11. 4 generations backK170332 Digital Radiography Cxdi-710C Wireless, Digital Radiography…Canon, Inc. · 2017
  12. 3 generations backK212553 DIGITAL RADIOGRAPHY CXDI-Pro, D1Canon, Inc. · 2021
  13. 2 generations backK220098 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
  14. 1 generation backK221876 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
  15. This deviceK222855 Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−13K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−12K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−11K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−10K060433Digital Radiography Cxdi-50CCanon, Inc.2006—
−9K091545Digital Radiography Cxdi-60CCanon, Inc.2009—
−8K102012Digital RadiographyCanon Inc. -Medical Equipment Group20101
−7K103591Digital RadiographyCanon Inc. -Medical Equipment Group2011—
−6K112309Digital RadiographyCanon Inc. -Medical Equipment Group2011—
−5K131106Digital Radiography Cxdi-701C Wireless, Digital Radiography Cxdi-70IG…Canon, Inc.2013—
−4K170332Digital Radiography Cxdi-710C Wireless, Digital Radiography Cxdi-810C WirelessCanon, Inc.2017—
−3K212553DIGITAL RADIOGRAPHY CXDI-Pro, D1Canon, Inc.2021—
−2K220098Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc.2022—
−1K221876Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc.2022—
0 (this device)K222855Digital Radiography CXDI-Pro, Digital Radiography D1Canon, Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200310
200510
200610
200810
200910
FIG. 1 — Lineage of K222855, 1998–2022Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
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
*K221876Digital Radiography CXDI-Pro, Digital Radiography D1
Summary page 4
…MQB Regulation: 892.1680, Stationary X-ray System Class: II Predicate Device: Clearance: K221876 Manufacturer: Canon Inc. Trade Name: DIGITAL RADIOGRAPHY CXDI-Pro…
Canon, Inc.2022—

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 3 companies; a new generation was cleared every 1.2 years on median.
  • 1 of the 20 ancestors has a recall of any class.

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. 2022, 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?

The DIGITAL RADIOGRAPHY CXDI-Pro / D1 provides digital image capture for conventional film/screen radiographic examinations. This device is intended to capture, for display, radiographic images of human anatomy, and 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. “K222855: Digital Radiography CXDI-Pro, Digital Radiography D1.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222855

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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