510(k) · Cleared
Cleared0909FCC, 0909FCC-HS
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Rayence Co., Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Cleared on Mar 7, 2024 as substantially equivalent to K212753 (Rayence Co., Ltd., 2021) after a 29-day review. Its family tree reaches back 9 generations to 1998. 1 later device descends from it.
- Decided
- Mar 7, 2024
- Review
- 29 days
- Class
- Class II
- Product code
- MQB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 9 generations to K981556 (1998). 10 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 9 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
- 5 generations between
- 3 generations backK162518 1012WCC, 1012WGCRayence Co., Ltd. · 2016
- 2 generations backK202722 1212FCARayence Co., Ltd. · 2020
- 1 generation backK212753 0909FCB, 1212FCARayence Co., Ltd. · 2021
- This deviceK240371 0909FCC, 0909FCC-HSRayence Co., Ltd. · 2024
- Descendant · cites it directly · 0 of its ownK253800 0909FCE, 0909FCE-HSRayence Co., Ltd. · 2026
Show all 9 generations
- Root · 9 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
- 8 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
- 7 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
- 6 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
- 5 generations backK101590 Digital Flat Panel X-Ray DetectorVATECH Co., Ltd. · 2010
- 4 generations backK123345 Digital Flat Panel X-Ray Detector / 1012WCARayence Co., Ltd. · 2013
- 3 generations backK162518 1012WCC, 1012WGCRayence Co., Ltd. · 2016
- 2 generations backK202722 1212FCARayence Co., Ltd. · 2020
- 1 generation backK212753 0909FCB, 1212FCARayence Co., Ltd. · 2021
- This deviceK240371 0909FCC, 0909FCC-HSRayence Co., Ltd. · 2024
Most influential descendants
Showing 1 of 1 · See all- K2538000909FCE, 0909FCE-HSRayence Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K981556 | Canon X-Ray Digital Camera Cxdi-11 | Canon USA, Inc. | 1998 | — |
| −8 | K992547 | Canon X-Ray Digital Camera, Model Cxdi-22 | Canon USA, Inc. | 1999 | — |
| −7 | K023750 | Cannon Digital Radiography Model Cxdi-40G | Canon USA, Inc. | 2002 | — |
| −6 | K031447 | Canon, Digital Radiography, Model Cxdi-50G | Canon, Inc. | 2003 | — |
| −5 | K101590 | Digital Flat Panel X-Ray Detector | VATECH Co., Ltd. | 2010 | — |
| −4 | K123345 | Digital Flat Panel X-Ray Detector / 1012WCA | Rayence Co., Ltd. | 2013 | — |
| −3 | K162518 | 1012WCC, 1012WGC | Rayence Co., Ltd. | 2016 | — |
| −2 | K202722 | 1212FCA | Rayence Co., Ltd. | 2020 | — |
| −1 | K212753 | 0909FCB, 1212FCA | Rayence Co., Ltd. | 2021 | — |
| 0 (this device) | K240371 | 0909FCC, 0909FCC-HS | Rayence Co., Ltd. | 2024 | — |
| +1 | K253800 | 0909FCE, 0909FCE-HS | Rayence Co., Ltd. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2026 | 1 | 0 |
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 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K212753 | 0909FCB, 1212FCASummary page 4…Device : Trade/Device Name :1212FCA Common Name : Digital Flat Panel X-ray Detector 510(k) Number : K212753 Regulation Number : 21 CFR 892.1680 Regulation Name : Stationary X-ray System… | 2021 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K253800 | 0909FCE, 0909FCE-HS | 2026 | 0 |
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 26 years and passes through 4 companies; a new generation was cleared every 2.4 years on median.
- None of the 10 ancestors has a recall.
- Of its descendants, K253800 (Rayence Co., Ltd., 2026) has gone furthest, with 0 descendants of its own.
How does its category compare?
All MQB devicesMQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · MQB
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MQB
127in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQB
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQB
141in 2025
MAUDE reports naming product code MQB, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 13 | 22 | 15 | 25 |
| 2008 | 8 | 15 | 36 | 30 |
| 2009 | 15 | 57 | 19 | 34 |
| 2010 | 11 | 116 | 14 | 39 |
| 2011 | 24 | 102 | 10 | 101 |
| 2012 | 22 | 80 | 8 | 267 |
| 2013 | 21 | 105 | 6 | 159 |
| 2014 | 32 | 102 | 0 | 29 |
| 2015 | 21 | 81 | 0 | 21 |
| 2016 | 22 | 92 | 0 | 26 |
| 2017 | 31 | 30 | 1 | 20 |
| 2018 | 16 | 30 | 4 | 84 |
| 2019 | 22 | 30 | 1 | 45 |
| 2020 | 19 | 28 | 4 | 9 |
| 2021 | 21 | 48 | 1 | 26 |
| 2022 | 31 | 48 | 0 | 13 |
| 2023 | 10 | 30 | 0 | 51 |
| 2024 | 8 | 187 | 0 | 91 |
| 2025 | 8 | 127 | 1 | 141 |
| 2026 | 3 | 245 | 1 | — |
What is it indicated for?
“0909FCC and 0909FCC-HS are indicated for digital imaging solution designed including head, neck, cervical spine, arm, leg and peripheral (foot, hand, wrist, fingers, etc.). The detectors are intended to replace the x-ray imager on film based radiographic diagnostic systems. Not to be used for mammography.”
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K240371 · printed Nov 4, 2026
Cite this page
510(k) Report. “K240371: 0909FCC, 0909FCC-HS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K240371
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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