510(k) Report

510(k) · Cleared

Cleared

Mercu 1717V

K222886510(k) SpecialCleared Oct 20, 202227-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

Iray Technology Taicang, Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Oct 20, 2022 as substantially equivalent to K221714 (Iray Technology Taicang, Ltd., 2022) after a 27-day review. Its family tree reaches back 15 generations to 1998.

Decided
Oct 20, 2022
Review
27 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 15 generations to K981556 (1998). 26 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 15 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 11 generations between
  3. 3 generations backK183713 Wireless Digital Flat DetectorIray Technology Taicang, Ltd. · 2019
  4. 2 generations backK201043 Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W)Iray Technology Taicang, Ltd. · 2020
  5. 1 generation backK221714 Flat Panel DetectorIray Technology Taicang, Ltd. · 2022
  6. This deviceK222886 Mercu 1717VIray Technology Taicang, Ltd. · 2022
Show all 15 generations
  1. Root · 15 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 14 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 13 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 12 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 11 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
  6. 10 generations backK082604 Viztek DR, Models: DR1000, DR3000, DR4000Viztek, Inc. · 2008
  7. 9 generations backK102123 Vizion DRViztek, Inc. · 2011
  8. 8 generations backK112661 Vizion DRViztek, LLC · 2011
  9. 7 generations backK123644 Vizion + DRViztek, LLC · 2013
  10. 6 generations backK152279 ViZion DR + WirelessViztek, LLC · 2015
  11. 5 generations backK161730 Wireless Digital Flat Panel DetectorIray Technology (Shanghai), Ltd. · 2016
  12. 4 generations backK182551 Wireless Digital Flat Panel DetectorIray Technology Taicang, Ltd. · 2018
  13. 3 generations backK183713 Wireless Digital Flat DetectorIray Technology Taicang, Ltd. · 2019
  14. 2 generations backK201043 Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W)Iray Technology Taicang, Ltd. · 2020
  15. 1 generation backK221714 Flat Panel DetectorIray Technology Taicang, Ltd. · 2022
  16. This deviceK222886 Mercu 1717VIray Technology Taicang, Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−15K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−14K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−13K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−12K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−11K042876Urs LP Digital, Millennium, RadproSedecal., Sa.2004—
−10K082604Viztek DR, Models: DR1000, DR3000, DR4000Viztek, Inc.2008—
−9K102123Vizion DRViztek, Inc.2011—
−8K112661Vizion DRViztek, LLC2011—
−7K123644Vizion + DRViztek, LLC2013—
−6K152279ViZion DR + WirelessViztek, LLC2015—
−5K161730Wireless Digital Flat Panel DetectorIray Technology (Shanghai), Ltd.2016—
−4K182551Wireless Digital Flat Panel DetectorIray Technology Taicang, Ltd.2018—
−3K183713Wireless Digital Flat DetectorIray Technology Taicang, Ltd.2019—
−2K201043Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W)Iray Technology Taicang, Ltd.2020—
−1K221714Flat Panel DetectorIray Technology Taicang, Ltd.2022—
0 (this device)K222886Mercu 1717VIray Technology Taicang, Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200140
200210
200310
200610
200710
200810
201210
FIG. 1 — Lineage of K222886, 1998–2022Source: 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
*K221714Flat Panel Detector
Summary page 5
…Stationary X-Ray System Regulation Number: 21 CFR 892.1680 Device Class: Class II FDA 510 (k) #: K221714 5. Identification of Reference Devices(s) [21 CFR 807.92(a)(3)] Manufacturer: CareRay Digital Medical Tech…
Iray Technology Taicang, Ltd.2022—
†K202995X-ray Flat Panel Detectors/CareView 3600RFCareray Digital Medical System Co., Ltd.2021—

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 7 companies; a new generation was cleared every 1.3 years on median.
  • 1 of the 26 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?

Mercu1717V Digital Flat Panel Detector is indicated for digital imaging solutions designed to provide general radiographic diagnosis for human anatomy including both adult and pediatric patients. It is intended to replace film/screen systems in all general–purpose diagnostic procedures. The device is not intended for mammography or dental applications.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222886: Mercu 1717V.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222886

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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