510(k) · Cleared
ClearedFUJIFILM Duodenoscope Model
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Fujifilm Corporation · FDT Duodenoscope And Accessories, Flexible/Rigid
Cleared on Mar 28, 2019 as substantially equivalent to K152257 (Fujifilm Medical Systems U.S.A, Inc., 2017) after a 269-day review. Its family tree reaches back 3 generations to 1995. 3 later devices descend from it.
- Decided
- Mar 28, 2019
- Review
- 269 days
- Class
- Class II
- Product code
- FDT
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K944759 (1995). 4 ancestors in all. 3 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK944759 200 Series Gastro-Intestinal Video SystemFujinon, Inc. · 1995 · Recalled
- 2 generations backK042076 Fujinon G5 Duodenscopes; G5 Duodenoscopes, ED-450XT5, ED-250XT5Fujinon, Inc. · 2004 · Recalled
- 1 generation backK152257 Fujifilm Duodenoscope Model ED-530XTFujifilm Medical Systems U.S.A, Inc. · 2017 · Recalled
- This deviceK181745 FUJIFILM Duodenoscope ModelFujifilm Corporation · 2019
- Descendant · cites it directly · 2 of its ownK191747 FUJIFILM Duodenoscope Model ED-580XTFujifilm Corporation · 2019
- Descendant · 2 generations on · 0 of its ownK251861 FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model…Fujifilm Corporation · 2026
- Descendant · 2 generations on · 0 of its ownK203028 FUJIFILM Distal End CapFujifilm Corporation · 2020
Most influential descendants
Showing 3 of 3 · See all- K191747FUJIFILM Duodenoscope Model ED-580XTFujifilm Corporation · 2019 · cites it directly2descendants
- K251861FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model ED-S100XP; FUJIFILM…Fujifilm Corporation · 2026 · 2 generations on0descendants
- K203028FUJIFILM Distal End CapFujifilm Corporation · 2020 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K944759 | 200 Series Gastro-Intestinal Video System | Fujinon, Inc. | 1995 | 5 |
| −2 | K042076 | Fujinon G5 Duodenscopes; G5 Duodenoscopes, ED-450XT5, ED-250XT5 | Fujinon, Inc. | 2004 | 4 |
| −1 | K152257 | Fujifilm Duodenoscope Model ED-530XT | Fujifilm Medical Systems U.S.A, Inc. | 2017 | 3 |
| 0 (this device) | K181745 | FUJIFILM Duodenoscope Model | Fujifilm Corporation | 2019 | — |
| +1 | K191747 | FUJIFILM Duodenoscope Model ED-580XT | Fujifilm Corporation | 2019 | — |
| +2 | K251861 | FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model ED-S100XP… | Fujifilm Corporation | 2026 | — |
| +2 | K203028 | FUJIFILM Distal End Cap | Fujifilm Corporation | 2020 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2026 | 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 FDT? 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 FDT device
- #1 K251861 FUJIFILM Endoscope Model ED-S100TP; FUJIFILM…score 13.7 · 10 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 |
|---|---|---|---|
| * | K152257 | Fujifilm Duodenoscope Model ED-530XTSummary page 4…ssification Name: Endoscope and accessories CFR Section: 21 CFR 876.1500 Product Code: FDT Predicate Device: FUJIFILM Duodenoscope Model ED-530XT (K152257) Reference Devices: FUJIFILM Endoscope Model EC-760R-V/L (K172916) EVIS EXERA II Duodenovideoscope Olympus TJF Ty… | 2017 |
| † | K172916 | FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and FUJIFILM… | 2018 |
| † | K143153 | Evis Exera II Duodenovideoscope Olympus TJF Type Q180V | 2016 |
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 |
|---|---|---|---|
| K191747 | FUJIFILM Duodenoscope Model ED-580XT | 2019 | 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 24 years and passes through 3 companies; a new generation was cleared every 9.6 years on median.
- 4 of the 4 ancestors have a recall of any class.
- Of its descendants, K191747 (Fujifilm Corporation, 2019) has gone furthest, with 2 descendants of its own.
- 1 other device also cites its predicate K152257.
How does its category compare?
All FDT devicesFDT Duodenoscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · FDT
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FDT
72in 2020
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FDT
7so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FDT
3,946in 2025
MAUDE reports naming product code FDT, 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 | 0 | — | 0 | 4 |
| 2008 | 1 | — | 0 | 11 |
| 2009 | 1 | — | 0 | 18 |
| 2010 | 0 | — | 0 | 12 |
| 2011 | 1 | — | 0 | 10 |
| 2012 | 0 | — | 0 | 15 |
| 2013 | 0 | — | 0 | 18 |
| 2014 | 0 | — | 0 | 36 |
| 2015 | 0 | — | 1 | 246 |
| 2016 | 1 | — | 1 | 247 |
| 2017 | 2 | — | 0 | 791 |
| 2018 | 3 | 63 | 1 | 481 |
| 2019 | 5 | 88 | 0 | 1,347 |
| 2020 | 4 | 72 | 0 | 822 |
| 2021 | 2 | — | 1 | 1,270 |
| 2022 | 1 | — | 0 | 2,619 |
| 2023 | 0 | — | 3 | 3,050 |
| 2024 | 2 | — | 0 | 3,019 |
| 2025 | 2 | — | 1 | 3,946 |
| 2026 | 2 | — | 7 | — |
What is it indicated for?
This device is intended for the visualization of the duodenum and upper digestive tract, specifically for the observation, diagnosis, and endoscopic treatment of the esophagus, stomach, and duodenum.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K181745 · printed Nov 6, 2026
Cite this page
510(k) Report. “K181745: FUJIFILM Duodenoscope Model.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181745
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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