510(k) Report

510(k) · Cleared

Cleared

2MP Monochrome LCD Monitor, Radiforce GX240

K120407510(k) TraditionalCleared Apr 19, 201270-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Eizo Nanao Corporation · LLZ System, Image Processing, Radiological

Cleared on Apr 19, 2012 as substantially equivalent to K070131 (Eizo Nanao Corporation, 2007) after a 70-day review. Its family tree reaches back 5 generations to 2000. 4 later devices descend from it.

Decided
Apr 19, 2012
Review
70 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K000293 (2000). 4 later devices descend from it, 3 citing it directly.

  1. Root · 5 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 4 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 3 generations backK022109 Eizo, Model FC-2091Eizo Nanao Corporation · 2002
  4. 2 generations backK041597 Monochrome LCD Monitor, Model Radiforce G22Eizo Nanao Corporation · 2004
  5. 1 generation backK070131 Radiforce GX220 and GS220 Monochrome LCD MonitorsEizo Nanao Corporation · 2007
  6. This deviceK120407 2MP Monochrome LCD Monitor, Radiforce GX240Eizo Nanao Corporation · 2012
  7. Descendant · cites it directly · 1 of its ownK172815 2MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd. · 2017
  8. Descendant · 2 generations on · 0 of its ownK253242 LCD Monitor (C1216W, C822W, C821W)Shenzhen Beacon Display Technology Co., Ltd. · 2025
  9. Descendant · cites it directly · 0 of its ownK201599 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+…Shenzhen Beacon Display Technology Co., Ltd. · 2020
  10. Descendant · cites it directly · 0 of its ownK151238 JUSHA-M23C LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2015

Most influential descendants

Showing 4 of 4 · See all
  • K1728152MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd. · 2017 · cites it directly1descendant
  • K253242LCD Monitor (C1216W, C822W, C821W)Shenzhen Beacon Display Technology Co., Ltd. · 2025 · 2 generations on0descendants
  • K2015992MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+Shenzhen Beacon Display Technology Co., Ltd. · 2020 · cites it directly0descendants
  • K151238JUSHA-M23C LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−4K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−3K022109Eizo, Model FC-2091Eizo Nanao Corporation2002—
−2K041597Monochrome LCD Monitor, Model Radiforce G22Eizo Nanao Corporation2004—
−1K070131Radiforce GX220 and GS220 Monochrome LCD MonitorsEizo Nanao Corporation2007—
0 (this device)K1204072MP Monochrome LCD Monitor, Radiforce GX240Eizo Nanao Corporation2012—
+1K1728152MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd.2017—
+2K253242LCD Monitor (C1216W, C822W, C821W)Shenzhen Beacon Display Technology Co., Ltd.2025—
+1K2015992MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+Shenzhen Beacon Display Technology Co., Ltd.2020—
+1K151238JUSHA-M23C LCD MonitorNanjing Jusha Display Technology Co., Ltd.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201710
202010
202510
FIG. 1 — Lineage of K120407, 2000–2025Source: 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 LLZ? 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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
*K070131Radiforce GX220 and GS220 Monochrome LCD Monitors
Summary page 1
…Processing, Radiological * Regulation Number: 21 CFR 892.2050, Product Code LLZ 5. Predicate Device * Monochrome LCD Monitor, RadiForce 65220 (K070131) 6. Device Description The RadiForce GX240 is a monochrome LCD monitor for viewing medical images other than those of mammograph…
Eizo Nanao Corporation2007—

What descends from it? (4)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K1728152MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd.20171
K2015992MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+Shenzhen Beacon Display Technology Co., Ltd.20200
K151238JUSHA-M23C LCD MonitorNanjing Jusha Display Technology Co., Ltd.20150

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 12 years and passes through 3 companies; a new generation was cleared every 2.0 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K172815 (Shenzhen Beacon Display Technology Co., Ltd., 2017) has gone furthest, with 1 descendant of its own.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

The RadiForce UX240 is intended to be used in displaying and viewing digital images by trained medical practitioners. The RadiForce GX240 does not support the display of mammography images for diagnosis.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120407: 2MP Monochrome LCD Monitor, Radiforce GX240.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K120407

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