510(k) · Cleared

Cleared

Radiforce RX240

K113844510(k) TraditionalCleared Feb 27, 201261-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 Feb 27, 2012 as substantially equivalent to K092613 (Eizo Nanao Corporation, 2010) after a 61-day review. Its family tree reaches back 1 generation to 2010. 11 later devices descend from it.

Decided: Feb 27, 2012
Review: 61 days
Class: Class II
Product code: LLZ
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K092613 (2010). 11 later devices descend from it, 3 citing it directly.

By dateBy generation

Root · 1 generation backK092613 Color LCD Monitor, Model Radiforce RS210Eizo Nanao Corporation · 2010
This deviceK113844 Radiforce RX240Eizo Nanao Corporation · 2012
Descendant · cites it directly · 5 of its ownK150106 2MP Color LCD Monitor, RadiForce RS240Eizo Corporation · 2015
Descendant · 2 generations on · 4 of its ownK160247 2MP Color LCD Monitor, RadiForce RX250 and RX250-AREizo Corporation · 2016
Descendant · cites it directly · 3 of its ownK151861 JUSHA-C23C LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2015
Descendant · 2 generations on · 2 of its ownK183498 JUSHA-C270G/ JUSHA-C270/ C270G/ C270 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2019
Descendant · 3 generations on · 1 of its ownK172815 2MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd. · 2017

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2015high 3 (2023) · low 0 (2018)2026

Most influential descendants

Showing 5 of 11 · See all

K1501062MP Color LCD Monitor, RadiForce RS240Eizo Corporation · 2015 · cites it directly5descendants
K1602472MP Color LCD Monitor, RadiForce RX250 and RX250-AREizo Corporation · 2016 · 2 generations on4descendants
K151861JUSHA-C23C LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2015 · cites it directly3descendants
K183498JUSHA-C270G/ JUSHA-C270/ C270G/ C270 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2019 · 2 generations on2descendants
K1728152MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)Shenzhen Beacon Display Technology Co., Ltd. · 2017 · 3 generations on1descendant

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K092613	Color LCD Monitor, Model Radiforce RS210	Eizo Nanao Corporation	2010	—
0 (this device)	K113844	Radiforce RX240	Eizo Nanao Corporation	2012	—
+1	K150106	2MP Color LCD Monitor, RadiForce RS240	Eizo Corporation	2015	—
+2	K160247	2MP Color LCD Monitor, RadiForce RX250 and RX250-AR	Eizo Corporation	2016	—
+1	K151861	JUSHA-C23C LCD Monitor	Nanjing Jusha Display Technology Co., Ltd.	2015	—
+2	K183498	JUSHA-C270G/ JUSHA-C270/ C270G/ C270 LCD Monitor	Nanjing Jusha Display Technology Co., Ltd.	2019	—
+3	K172815	2MP LCD Monitor (G22S+, G22SP+, C22S+, C22SP+)	Shenzhen Beacon Display Technology Co., Ltd.	2017	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2015	2	0
2016	1	0
2017	1	0
2019	1	0
2020	1	0
2022	1	0
2023	3	0
2025	1	0

FIG. 1 — Lineage of K113844, 2010–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
#2 Held for the reportin the report
#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.

Type	Number	Device	Applicant	Decided	Recalls
*	K092613	Color LCD Monitor, Model Radiforce RS210 Summary page 1 …age Processing, Radiological " Classification Number: 21 CFR 892.2050, Product Code LLZ 5. Predicate Device * Color LCD Monitor, RadiForce RS210 (K092613) 6. Device Description The RadiForce RX240 is a color LCD monitor for viewing medical images other than those of mammography. Th…	Eizo Nanao Corporation	2010	—

Also cleared against K092613: 2 other devices →

What descends from it? (11)

See all 11

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

Number	Device	Applicant	Decided	Descendants
K150106	2MP Color LCD Monitor, RadiForce RS240	Eizo Corporation	2015	5
K151861	JUSHA-C23C LCD Monitor	Nanjing Jusha Display Technology Co., Ltd.	2015	3
K233465	RadiForce MX317W	Eizo Corporation	2023	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?

Its one ancestor has no recall.
Of its descendants, K150106 (Eizo Corporation, 2015) has gone furthest, with 5 descendants of its own.
2 other devices also cite its predicate K092613.

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

2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

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

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

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	76	36	20	152
2008	94	52	32	154
2009	70	62	21	145
2010	51	98	17	145
2011	106	79	30	454
2012	82	87	12	266
2013	95	84	64	1,130
2014	78	89	6	15,631
2015	64	90	16	211
2016	82	90	12	290
2017	78	107	5	104
2018	104	105	7	72
2019	74	107	2	88
2020	81	115	6	82
2021	83	116	3	70
2022	65	137	4	28
2023	87	157	8	26
2024	62	131	6	42
2025	58	173	11	116
2026	45	110	14	—

What is it indicated for?

The RadiForce RX240 is intended to be used in displaying and viewing digital images

for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The device does

not support the display of mammography images for diagnosis.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K113844 · printed Nov 6, 2026

Cite this page

510(k) Report. “K113844: Radiforce RX240.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113844

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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