510(k) Report

510(k) · Cleared

Cleared

Color LCD Monitor, Model Radiforce RS210

K092613510(k) SpecialCleared Mar 3, 2010189-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 Mar 3, 2010 after a 189-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 27 later devices descend from it.

Decided
Mar 3, 2010
Review
189 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
0

27 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2012: 2 descendants cleared2013: 1 descendant cleared2014: 1 descendant cleared2015: 2 descendants cleared2023: 7 descendants cleared2019: 2 descendants cleared2020: 2 descendants cleared2018: 1 descendant cleared2022: 3 descendants cleared2016: 1 descendant cleared2025: 2 descendants cleared2017: 1 descendant cleared2026: 2 descendants cleared2010201520202025
  1. This deviceK092613 Color LCD Monitor, Model Radiforce RS210Eizo Nanao Corporation · 2010
  2. Descendant · cites it directly · 11 of its ownK113844 Radiforce RX240Eizo Nanao Corporation · 2012
  3. Descendant · cites it directly · 8 of its ownK131090 2MP Color LCD Monitor, Radiforce MX215Eizo Corporation · 2013
  4. Descendant · 2 generations on · 5 of its ownK150106 2MP Color LCD Monitor, RadiForce RS240Eizo Corporation · 2015
  5. Descendant · cites it directly · 5 of its ownK113240 3.7 MP Color LCD Monitor, Radiforce MX270WEizo Nanao Corporation · 2012
  6. Descendant · 3 generations on · 4 of its ownK160247 2MP Color LCD Monitor, RadiForce RX250 and RX250-AREizo Corporation · 2016

Showing 5 of 27 descendants. See all descendants

Descendants cleared per year

2012: 22013: 12014: 12015: 22016: 12017: 12018: 12019: 22020: 22022: 32023: 72025: 22026: 2
2012high 7 (2023) · low 0 (2021)2026

Most influential descendants

Showing 5 of 27 · See all
  • K113844Radiforce RX240Eizo Nanao Corporation · 2012 · cites it directly11descendants
  • K1310902MP Color LCD Monitor, Radiforce MX215Eizo Corporation · 2013 · cites it directly8descendants
  • K1501062MP Color LCD Monitor, RadiForce RS240Eizo Corporation · 2015 · 2 generations on5descendants
  • K1132403.7 MP Color LCD Monitor, Radiforce MX270WEizo Nanao Corporation · 2012 · cites it directly5descendants
  • K1602472MP Color LCD Monitor, RadiForce RX250 and RX250-AREizo Corporation · 2016 · 3 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K092613Color LCD Monitor, Model Radiforce RS210Eizo Nanao Corporation2010—
+1K113844Radiforce RX240Eizo Nanao Corporation2012—
+1K1310902MP Color LCD Monitor, Radiforce MX215Eizo Corporation2013—
+2K1501062MP Color LCD Monitor, RadiForce RS240Eizo Corporation2015—
+1K1132403.7 MP Color LCD Monitor, Radiforce MX270WEizo Nanao Corporation2012—
+3K1602472MP Color LCD Monitor, RadiForce RX250 and RX250-AREizo Corporation2016—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201220
201310
201410
201520
201610
201710
201810
201920
202020
202230
202370
202520
202620
FIG. 1 — Lineage of K092613, 2010–2026Source: 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 510(k) statement (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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (27)

See all 27

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

NumberDeviceApplicantDecidedDescendants
K113844Radiforce RX240Eizo Nanao Corporation201211
K1310902MP Color LCD Monitor, Radiforce MX215Eizo Corporation20138
K1132403.7 MP Color LCD Monitor, Radiforce MX270WEizo Nanao Corporation20125

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?

  • Of its descendants, K113844 (Eizo Nanao Corporation, 2012) has gone furthest, with 11 descendants 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. 2010, 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?

RadiForce RS21O is intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. RadiForce RS21O does not support the display of mammography images for diagnosis.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K092613: Color LCD Monitor, Model Radiforce RS210.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K092613

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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