510(k) · Cleared
ClearedSony LMD-2451MT LCD Monitor
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sony Electronics, Inc. · GCJ Laparoscope, General & Plastic Surgery
Cleared on Feb 24, 2012 as substantially equivalent to K102379 (Olympus Medical Systems Corporation, 2011) after a 116-day review. Its family tree reaches back 2 generations to 1995. 12 later devices descend from it.
- Decided
- Feb 24, 2012
- Review
- 116 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K943305 (1995). 5 ancestors in all. 12 later devices descend from it, 3 citing it directly.
- Root · 2 generations backK943305 Olympus 3D Surgical Endoscopy SystemOlympus America, Inc. · 1995
- 1 generation backK102379 LTF-Y0009; Maj-YOO41; Xoev-3D1Olympus Medical Systems Corporation · 2011
- This deviceK113203 Sony LMD-2451MT LCD MonitorSony Electronics, Inc. · 2012
- Descendant · cites it directly · 9 of its ownK150377 Sony LMD-X310S LCD Monitor, Sony LMD-X310MD LCD Monitor, Sony…Sony Electronics, Inc. · 2015
- Descendant · 2 generations on · 7 of its ownK220069 4K UHD LCD Monitor OEV321UHOlympus Medical Systems Corp. · 2022 · Recalled
- Descendant · 3 generations on · 5 of its ownK231066 CuratOR EX3242-FDEizo Corporation · 2023
- Descendant · cites it directly · 4 of its ownK170899 27HJ713SLg Electronics · 2017
- Descendant · 2 generations on · 3 of its ownK241402 Medical Monitor (32HR734S)Lg Electronics.Inc · 2024
Showing 5 of 12 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 12 · See all- K150377Sony LMD-X310S LCD Monitor, Sony LMD-X310MD LCD Monitor, Sony LMD-X310NB LCD Monitor…Sony Electronics, Inc. · 2015 · cites it directly9descendants
- K2200694K UHD LCD Monitor OEV321UHOlympus Medical Systems Corp. · 2022 · 2 generations on7descendants
- K231066CuratOR EX3242-FDEizo Corporation · 2023 · 3 generations on5descendants
- K17089927HJ713SLg Electronics · 2017 · cites it directly4descendants
- K241402Medical Monitor (32HR734S)Lg Electronics.Inc · 2024 · 2 generations on3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K943305 | Olympus 3D Surgical Endoscopy System | Olympus America, Inc. | 1995 | — |
| −1 | K102379 | LTF-Y0009; Maj-YOO41; Xoev-3D1 | Olympus Medical Systems Corporation | 2011 | — |
| 0 (this device) | K113203 | Sony LMD-2451MT LCD Monitor | Sony Electronics, Inc. | 2012 | — |
| +1 | K150377 | Sony LMD-X310S LCD Monitor, Sony LMD-X310MD LCD Monitor, Sony LMD-X310NB LCD… | Sony Electronics, Inc. | 2015 | — |
| +2 | K220069 | 4K UHD LCD Monitor OEV321UH | Olympus Medical Systems Corp. | 2022 | 1 |
| +3 | K231066 | CuratOR EX3242-FD | Eizo Corporation | 2023 | — |
| +1 | K170899 | 27HJ713S | Lg Electronics | 2017 | — |
| +2 | K241402 | Medical Monitor (32HR734S) | Lg Electronics.Inc | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 2 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
| 2019 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 2 | 0 |
| 2025 | 2 | 0 |
| 2026 | 3 | 0 |
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 GCJ? 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 GCJ device
- #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 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 |
|---|---|---|---|
| * | K102379 | LTF-Y0009; Maj-YOO41; Xoev-3D1Summary page 1…Classification Name: Endoscope and Accessories 3. PREDICATE DEVICE *Polarized 3D Monitor XOEV-3D1, Olympus Medical Systems Corporation, K102379 4. DEVICE DESCRIPTION The Sony LMD-2451MT LCD Monitor is intended primarily for use in a medical environment for d… | 2011 |
What descends from it? (12)
See all 123 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 17 years and passes through 3 companies; a new generation was cleared every 15.1 years on median.
- None of the 5 ancestors has a recall.
- Of its descendants, K150377 (Sony Electronics, Inc., 2015) has gone furthest, with 9 descendants of its own.
- 1 other device also cites its predicate K102379.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · GCJ
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GCJ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GCJ
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GCJ
5,860in 2025
MAUDE reports naming product code GCJ, 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 | 18 | 42 | 12 | 1,639 |
| 2008 | 19 | 73 | 16 | 1,319 |
| 2009 | 21 | 85 | 6 | 1,995 |
| 2010 | 24 | 122 | 30 | 2,657 |
| 2011 | 15 | 113 | 9 | 2,133 |
| 2012 | 17 | 88 | 1 | 1,526 |
| 2013 | 15 | 93 | 7 (1) | 1,565 |
| 2014 | 19 | 90 | 2 | 1,714 |
| 2015 | 26 | 76 | 0 | 1,710 |
| 2016 | 27 | 99 | 5 | 2,080 |
| 2017 | 20 | 77 | 1 | 3,468 |
| 2018 | 21 | 88 | 1 | 2,562 |
| 2019 | 15 | 60 | 0 | 2,578 |
| 2020 | 28 | 61 | 0 | 2,618 |
| 2021 | 18 | 116 | 0 | 3,431 |
| 2022 | 20 | 103 | 1 | 3,945 |
| 2023 | 31 | 109 | 1 | 6,002 |
| 2024 | 29 | 90 | 0 | 6,047 |
| 2025 | 21 | 108 | 5 | 5,860 |
| 2026 | 26 | 122 | 1 | — |
What is it indicated for?
The Sony LMD-2451MT LCD Monitor is intended to provide 3D and 2D color video displays of images from surgical endoscopic/laparoscopic camera systems and other compatible medical imaging systems. The LMD-2451MT is a widescreen, high-definition, medical grade monitor for real-time use during minimally invasive surgical procedures and is suitable for use in hospital operating rooms, surgical centers, clinics, doctors' offices and similar medical environments.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K113203 · printed Nov 6, 2026
Cite this page
510(k) Report. “K113203: Sony LMD-2451MT LCD Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113203
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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