510(k) · Cleared
ClearedPENTAX Medical ED34-i10T, Video Duodenoscope
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pentax Medical · FDT Duodenoscope And Accessories, Flexible/Rigid
Cleared on Sep 20, 2017 as substantially equivalent to K092710 (Pentax Medical Company, 2009) after a 272-day review. Its family tree reaches back 3 generations to 1983. 4 later devices descend from it.
- Decided
- Sep 20, 2017
- Review
- 272 days
- Class
- Class II
- Product code
- FDT
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K832006 (1983). 5 ancestors in all. 4 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK832006 Pentax FD-34A DuodenofiberscopePentax Precision Instrument Corp. · 1983
- 2 generations backK963056 ED-3410, Video DuodenoscopePentax Precision Instrument Corp. · 1996 · Recalled
- 1 generation backK092710 Pentax ED-3490TK, Video DuodenoscopePentax Medical Company · 2009 · Recalled
- This deviceK163614 PENTAX Medical ED34-i10T, Video DuodenoscopePentax Medical · 2017
- Descendant · cites it directly · 3 of its ownK192245 Pentax Medical Video Duodenoscope ED34-i10T2Pentax of America, Inc. · 2019 · Recalled
- Descendant · 2 generations on · 0 of its ownK233942 PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical…Pentax of America, Inc. · 2024
- Descendant · 2 generations on · 0 of its ownK210710 PENTAX Medical Video Duedenoscope ED34-i10T2Pentax of America, Inc. · 2021 · Recalled
- Descendant · 2 generations on · 0 of its ownK202365 Pentax Medical Video Duodenoscope ED32-i10Pentax of America, Inc. · 2021
Most influential descendants
Showing 4 of 4 · See all- K192245Pentax Medical Video Duodenoscope ED34-i10T2Pentax of America, Inc. · 2019 · cites it directly3descendants
- K233942PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor…Pentax of America, Inc. · 2024 · 2 generations on0descendants
- K210710PENTAX Medical Video Duedenoscope ED34-i10T2Pentax of America, Inc. · 2021 · 2 generations on0descendants
- K202365Pentax Medical Video Duodenoscope ED32-i10Pentax of America, Inc. · 2021 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K832006 | Pentax FD-34A Duodenofiberscope | Pentax Precision Instrument Corp. | 1983 | — |
| −2 | K963056 | ED-3410, Video Duodenoscope | Pentax Precision Instrument Corp. | 1996 | 2 |
| −1 | K092710 | Pentax ED-3490TK, Video Duodenoscope | Pentax Medical Company | 2009 | 2 |
| 0 (this device) | K163614 | PENTAX Medical ED34-i10T, Video Duodenoscope | Pentax Medical | 2017 | — |
| +1 | K192245 | Pentax Medical Video Duodenoscope ED34-i10T2 | Pentax of America, Inc. | 2019 | 1 |
| +2 | K233942 | PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video… | Pentax of America, Inc. | 2024 | — |
| +2 | K210710 | PENTAX Medical Video Duedenoscope ED34-i10T2 | Pentax of America, Inc. | 2021 | 1 |
| +2 | K202365 | Pentax Medical Video Duodenoscope ED32-i10 | Pentax of America, Inc. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2019 | 1 | 0 |
| 2021 | 2 | 0 |
| 2024 | 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 |
|---|---|---|---|
| * | K092710 | Pentax ED-3490TK, Video DuodenoscopeSummary page 4…cope and accessories Regulatory Class: Class II Product Code: FDT Predicate Device: PENTAX ED‐3490TK Video Duodenoscope (K092710, clearance received on December 2, 2009) Device Description: The ED34‐i10T, Video Duodenoscope i… | 2009 |
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K192245 | Pentax Medical Video Duodenoscope ED34-i10T2 | 2019 | 3 |
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 34 years and passes through 3 companies; a new generation was cleared every 13.1 years on median.
- 2 of the 5 ancestors have a recall of any class.
- Of its descendants, K192245 (Pentax of America, Inc., 2019) has gone furthest, with 3 descendants of its own.
- 1 other device also cites its predicate K092710.
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. 2017, 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?
The PENTAX Duodenoscope ED34-i10T is intended to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: Esophagus, Stomach, Duodenum, Common Bile, Hepatic and Cystic Ducts.
These instruments are introduced via the mouth when indications consistent with the need for the procedure are observed in adult and pediatric patient populations.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K163614 · printed Nov 6, 2026
Cite this page
510(k) Report. “K163614: PENTAX Medical ED34-i10T, Video Duodenoscope.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K163614
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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