510(k) Report

510(k) · Cleared

Cleared

LCD Monitors C310S, G310S, C316S, G316S, C616W

K240310510(k) TraditionalCleared Mar 29, 202456-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

Shenzhen Beacon Display Technology Co., Ltd. · PGY Display, Diagnostic Radiology

Cleared on Mar 29, 2024 as substantially equivalent to K201211 (Shenzhen Beacon Display Technology Co., Ltd., 2020) and 1 other predicate after a 56-day review. Its family tree reaches back 8 generations to 2000. 1 later device descends from it.

Decided
Mar 29, 2024
Review
56 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K000293 (2000). 16 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 8 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 7 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 6 generations backK022109 Eizo, Model FC-2091Eizo Nanao Corporation · 2002
  4. 5 generations backK052337 Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation · 2005
  5. 4 generations backK060845 Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation · 2006
  6. 3 generations backK062053 Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation · 2006
  7. 2 generations backK113784 3MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation · 2012
  8. 1 generation backK201211 3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors…Shenzhen Beacon Display Technology Co., Ltd. · 2020
  9. This deviceK240310 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024
  10. Descendant · cites it directly · 0 of its ownK243031 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−7K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−6K022109Eizo, Model FC-2091Eizo Nanao Corporation2002—
−5K052337Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation2005—
−4K060845Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation2006—
−3K062053Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation2006—
−2K1137843MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation2012—
−1K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+Shenzhen Beacon Display Technology Co., Ltd.2020—
0 (this device)K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—
+1K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
200910
201210
201410
201610
201820

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K240310, 2000–2024Source: 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 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 PGY? 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 PGY device

  1. #1 K261213 Medical Monitor (40HT513D)score 13.9 · 9 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? (2)

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
*K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+
Summary page 6
…s as follows: Shenzhen Beacon Display Technology Co., Ltd., 3MP Color LCD Monitors C32S+, 3MP Monochrome LCD Monitors G32S+has been cleared by FDA through 510(k) No. K201211 (Decision Date - 09/03/2020). Shenzhen Beacon Display Technology Co., Ltd., 6MP Color LCD Monitor (C61W+) has been cleared…
Shenzhen Beacon Display Technology Co., Ltd.2020—
*K1822916MP Color LCD Monitor (C61W+)
Summary page 6
…k) No. K201211 (Decision Date - 09/03/2020). Shenzhen Beacon Display Technology Co., Ltd., 6MP Color LCD Monitor (C61W+) has been cleared by FDA through 510(k) No. K182291 (Decision Date - 11/20/2018). 5. Description of the Device [21 CFR 807.92(a) (4)] 3MP LCD Monitors C310S, G310S, C316S, G31…
Shenzhen Beacon Display Technology Co., Ltd.2018—

Also cleared against K201211: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.20240

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 24 years and passes through 4 companies; a new generation was cleared every 3.2 years on median.
  • 2 of the 16 ancestors have a recall of any class.
  • Of its descendants, K243031 (Shenzhen Beacon Display Technology Co., Ltd., 2024) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K201211.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · PGY

3in 2025

2014: 142015: 162016: 182017: 112018: 52019: 112020: 122021: 72022: 102023: 172024: 102025: 32026 (partial year): 4
2007high 18 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PGY

59in 2025

2014: 24 days median2015: 31 days median2016: 27 days median2017: 30 days median2018: 28 days median2019: 58 days median2020: 61 days median2021: 77 days median2022: 60 days median2023: 60 days median2024: 53 days median2025: 59 days median2026 (partial year): 48 days median
2007high 77 (2021) · low 24 (2014)2026

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

Recalls per year · PGY

No recall names PGY since 2007.

Adverse event reports per year · PGY

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code PGY, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014142400
2015163100
2016182700
2017113001
201852800
2019115800
2020126100
202177700
2022106000
2023176000
2024105300
202535900
20264480—

What is it indicated for?

C310S, C316S and C616W are indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The displays are not intended for mammography.

G310S and G316S are intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The devices are not specified for digital mammography systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K240310: LCD Monitors C310S, G310S, C316S, G316S, C616W.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K240310

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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