510(k) · Cleared
ClearedPrudent 1717, Prudent 1417, Prudent 1212
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pixxgen Corporation · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Cleared on Jun 4, 2021 as substantially equivalent to K182533 (Pixxgen Corporation, 2018) after a 51-day review. Its family tree reaches back 6 generations to 2007.
- Decided
- Jun 4, 2021
- Review
- 51 days
- Class
- Class II
- Product code
- MQB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K063710 (2007). No later device cites it as a predicate yet.
- Root · 6 generations backK063710 Saturn 9000New Medical Co., Ltd. · 2007
- 5 generations backK080064 Flaatz 750Drtech Corp. · 2008
- 4 generations backK113812 ATAL-8Atlaim · 2012
- 3 generations backK152151 ATAL 9Atlaim Corporation · 2015
- 2 generations backK180976 PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor…Pixxgen Corporation · 2018
- 1 generation backK182533 PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor…Pixxgen Corporation · 2018
- This deviceK211108 Prudent 1717, Prudent 1417, Prudent 1212Pixxgen Corporation · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K063710 | Saturn 9000 | New Medical Co., Ltd. | 2007 | — |
| −5 | K080064 | Flaatz 750 | Drtech Corp. | 2008 | — |
| −4 | K113812 | ATAL-8 | Atlaim | 2012 | — |
| −3 | K152151 | ATAL 9 | Atlaim Corporation | 2015 | — |
| −2 | K180976 | PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels | Pixxgen Corporation | 2018 | — |
| −1 | K182533 | PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels | Pixxgen Corporation | 2018 | — |
| 0 (this device) | K211108 | Prudent 1717, Prudent 1417, Prudent 1212 | Pixxgen Corporation | 2021 | — |
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 |
|---|---|---|---|
| * | K182533 | PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor PanelsSummary page 4…Usual Name: Digital X-Ray Receptor Panel Device Class/Regulation Number: Class II per regulation 892.1680 Product Code: MQB 2. Equivalent legally marketed device: K182533 PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X- Ray Receptor Panels Classification Name: Solid State X-Ray Imager (F… | 2018 |
| † | K202995 | X-ray Flat Panel Detectors/CareView 3600RF | 2021 |
| † | K201932 | X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe) | 2020 |
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 14 years and passes through 5 companies; a new generation was cleared every 2.7 years on median.
- None of the 6 ancestors has a recall.
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. 2021, 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?
Indicated for use in general radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures, excluding fluoroscopic, angiographic, and mammographic applications.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K211108 · printed Nov 6, 2026
Cite this page
510(k) Report. “K211108: Prudent 1717, Prudent 1417, Prudent 1212.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211108
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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