510(k) · Cleared
ClearedEndocapsule Software 10; Endocapsule Software 10 Light
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Olympus Medical Systems Corp. · NEZ System, Imaging, Gastrointestinal, Wireless, Capsule
Cleared on Feb 8, 2015 as substantially equivalent to K123421 (Olympus Medical Systems Corp., 2013) after a 142-day review. Its family tree reaches back 2 generations to 2009. 3 later devices descend from it.
- Decided
- Feb 8, 2015
- Review
- 142 days
- Class
- Class II
- Product code
- NEZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K090210 (2009). 3 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK090210 Modification to Olympus Capsule Endoscope SystemOlympus Medical Systems Corporation · 2009
- 1 generation backK123421 Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2013
- This deviceK142680 Endocapsule Software 10; Endocapsule Software 10 LightOlympus Medical Systems Corp. · 2015
- Descendant · cites it directly · 2 of its ownK163069 Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2017
- Descendant · 2 generations on · 1 of its ownK173459 Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2018
- Descendant · 3 generations on · 0 of its ownK183053 Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2019
Most influential descendants
Showing 3 of 3 · See all- K163069Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2017 · cites it directly2descendants
- K173459Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2018 · 2 generations on1descendant
- K183053Olympus Small Intestinal Capsule Endoscope SystemOlympus Medical Systems Corp. · 2019 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K090210 | Modification to Olympus Capsule Endoscope System | Olympus Medical Systems Corporation | 2009 | — |
| −1 | K123421 | Olympus Small Intestinal Capsule Endoscope System | Olympus Medical Systems Corp. | 2013 | — |
| 0 (this device) | K142680 | Endocapsule Software 10; Endocapsule Software 10 Light | Olympus Medical Systems Corp. | 2015 | — |
| +1 | K163069 | Olympus Small Intestinal Capsule Endoscope System | Olympus Medical Systems Corp. | 2017 | — |
| +2 | K173459 | Olympus Small Intestinal Capsule Endoscope System | Olympus Medical Systems Corp. | 2018 | — |
| +3 | K183053 | Olympus Small Intestinal Capsule Endoscope System | Olympus Medical Systems Corp. | 2019 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 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 NEZ? 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 NEZ device
- #1 K252617 MiroCam® Capsule Endoscope Systemscore 17.0 · 20 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 |
|---|---|---|---|
| * | K123421 | Olympus Small Intestinal Capsule Endoscope SystemSummary page 5…ation Model name Applicant 510(k) No. OLYMPUS CAPSULE ENDOSCOPE OLYMPUS MEDICAL K123421 SYSTEM SYSTEMS CORP. IV. Device Description OLYMPUS SMALL INTESTINAL CA… | 2013 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K163069 | Olympus Small Intestinal Capsule Endoscope System | 2017 | 2 |
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 6 years and passes through 2 companies; a new generation was cleared every 3.8 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K163069 (Olympus Medical Systems Corp., 2017) has gone furthest, with 2 descendants of its own.
How does its category compare?
All NEZ devicesNEZ System, Imaging, Gastrointestinal, Wireless, Capsule: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · NEZ
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NEZ
99in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NEZ
1in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NEZ
69in 2025
MAUDE reports naming product code NEZ, 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 | 2 | — | 1 | 0 |
| 2008 | 0 | — | 0 | 9 |
| 2009 | 2 | — | 0 | 6 |
| 2010 | 1 | — | 0 | 13 |
| 2011 | 3 | 213 | 1 | 10 |
| 2012 | 1 | — | 0 | 19 |
| 2013 | 3 | 194 | 0 | 6 |
| 2014 | 3 | 194 | 0 | 13 |
| 2015 | 2 | — | 0 | 30 |
| 2016 | 2 | — | 0 | 57 |
| 2017 | 4 | 83 | 0 | 55 |
| 2018 | 3 | 233 | 0 | 50 |
| 2019 | 2 | — | 0 | 56 |
| 2020 | 1 | — | 0 | 31 |
| 2021 | 1 | — | 0 | 41 |
| 2022 | 1 | — | 0 | 63 |
| 2023 | 1 | — | 0 | 34 |
| 2024 | 3 | 99 | 0 | 103 |
| 2025 | 1 | — | 0 | 69 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The OLYMPUS SMALL INTESTINAL CAPSULE ENDOSCOPE SYSTEM is intended for visualization of the small intestine mucosa. The Red Color Detection Function is intended to mark frames of the video suspected of containing blood or red areas.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K142680 · printed Nov 6, 2026
Cite this page
510(k) Report. “K142680: Endocapsule Software 10; Endocapsule Software 10 Light.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142680
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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