510(k) Report

510(k) · Cleared

Cleared

Solid State X-Ray Imaging Device, Digital Flat Panel X-Ray Detector, 1417WGC

K141563510(k) SpecialCleared Jul 16, 201434-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

Rayence Co., Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Jul 16, 2014 as substantially equivalent to K131114 (Rayence Co., Ltd., 2013) after a 34-day review. Its family tree reaches back 7 generations to 1998.

Decided
Jul 16, 2014
Review
34 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K981556 (1998). 8 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 6 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 5 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 4 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 3 generations backK102321 Digital Flat Panel X-Ray Detector Model SDX-4336CPSamsung Mobile Display Co., Ltd. · 2011
  6. 2 generations backK122928 Digital Flat Panel X-Ray Detector/1417PGARayence Co., Ltd. · 2013
  7. 1 generation backK131114 Digital Flat Panel X-Ray DetectorRayence Co., Ltd. · 2013
  8. This deviceK141563 Solid State X-Ray Imaging Device, Digital Flat Panel X-Ray Detector…Rayence Co., Ltd. · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−6K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−5K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−4K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−3K102321Digital Flat Panel X-Ray Detector Model SDX-4336CPSamsung Mobile Display Co., Ltd.2011—
−2K122928Digital Flat Panel X-Ray Detector/1417PGARayence Co., Ltd.2013—
−1K131114Digital Flat Panel X-Ray DetectorRayence Co., Ltd.2013—
0 (this device)K141563Solid State X-Ray Imaging Device, Digital Flat Panel X-Ray Detector, 1417WGCRayence Co., Ltd.2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K141563, 1998–2014Source: 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
*K131114Digital Flat Panel X-Ray Detector
Summary page 2
…417WGC Predicate Device: Manufacturer Rayence Co., Ltd. Device 1417WGA 510(k) Number K 131 114 (Decision Date -September 17, 2013) Device Description 14I7WGC is a wired/wireless digital solid state X-ray detector tha…
Rayence Co., Ltd.2013—

Also cleared against K131114: 1 other device →

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 16 years and passes through 4 companies; a new generation was cleared every 11 months on median.
  • None of the 8 ancestors has a recall.
  • 1 other device also cites its predicate K131114.

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. 2014, 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?

I4I7WGC Digital Flat Panel X-Ray Detector is indicated for digital imaging solution designed for general radiographic system for human anatomy. It is intended to replace film or screen based radiographic systems in all general purpose diagnostic procedures. Not to be used for mammography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141563: Solid State X-Ray Imaging Device, Digital Flat Panel X-Ray Detector, 1417WGC.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141563

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