510(k) Report

510(k) · Cleared

Recalled · Class II · 2026

Trinias

K221922510(k) SpecialCleared Jul 28, 202227-day reviewClass II21 CFR 892.1650Recalls 1

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Shimadzu Corporation Medical Systems Division · OWB Interventional Fluoroscopic X-Ray System

Cleared on Jul 28, 2022 as substantially equivalent to K203535 (Shimadzu Corporation Medical Systems, 2021) after a 27-day review. Its family tree reaches back 2 generations to 2014. 1 later device descends from it. It has been recalled once.

Decided
Jul 28, 2022
Review
27 days
Class
Class II
Product code
OWB
Recalls
1
Predicates
1

Its longest line of descent runs back 2 generations to K123508 (2014). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2026: 1 descendant clearedK123508 · Trinias · Shimadzu Corporation · 2014 · recalledK203535 · Trinias · Shimadzu Corporation Medical Systems · 2021 · recalled2010201520202025
Descendants, by generation 1 generation forward: 1 descendant K203535 · Trinias · Shimadzu Corporation Medical Systems · 2021 · recalledK123508 · Trinias · Shimadzu Corporation · 2014 · recalled0
  1. Root · 2 generations backK123508 TriniasShimadzu Corporation · 2014 · Recalled
  2. 1 generation backK203535 TriniasShimadzu Corporation Medical Systems · 2021 · Recalled
  3. This deviceK221922 TriniasShimadzu Corporation Medical Systems Division · 2022
  4. Descendant · cites it directly · 0 of its ownK252099 TriniasShimadzu Corporation · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K252099TriniasShimadzu Corporation · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K123508TriniasShimadzu Corporation20148
−1K203535TriniasShimadzu Corporation Medical Systems20211
0 (this device)K221922TriniasShimadzu Corporation Medical Systems Division2022—
+1K252099TriniasShimadzu Corporation2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K221922, 2014–2026Source: 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 OWB? 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 OWB device

  1. #1 K251602 Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6…score 18.3 · 18 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K203535Trinias
Summary page 4
…roscopic x-ray system Regulatory Class: II Product Code: OWB Common/Usual Name: Interventional Fluoroscopic X-Ray System 2. Equivalent legally marketed device: K203535 Trade/Device Name: Trinias Manufacturer: Shimadzu. Regulation Number: 21CFR892.1650 Regulation Name: Image-intensifie…
Shimadzu Corporation Medical Systems20211

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K252099TriniasShimadzu Corporation20260

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Apr 20, 2026Class IIZ-2294-2026Component design/selectionElectromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 8 years and passes through 3 companies; a new generation was cleared every 7.2 years on median.
  • 2 of the 2 ancestors have a recall of any class.
  • Of its descendants, K252099 (Shimadzu Corporation, 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All OWB devices

OWB Interventional Fluoroscopic X-Ray System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · OWB

22in 2025

2007: 32008: 42009: 92010: 72011: 62012: 62013: 112014: 152015: 112016: 162017: 202018: 232019: 92020: 162021: 242022: 212023: 122024: 132025: 222026 (partial year): 15
2007high 24 (2021) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OWB

148in 2025

2007: 52 days median2008: 135 days median2009: 99 days median2010: 66 days median2011: 79 days median2012: 37 days median2013: 119 days median2014: 158 days median2015: 66 days median2016: 103 days median2017: 76 days median2018: 54 days median2019: 174 days median2020: 53 days median2021: 60 days median2022: 90 days median2023: 152 days median2024: 126 days median2025: 148 days median2026 (partial year): 221 days median
2007high 221 (2026) · low 37 (2012)2026

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

Recalls per year · OWB

42so far in 2026, the most since 2007

2008: 12013: 102014: 92015: 352016: 132017: 132018: 62019: 72020: 82021: 312022: 242023: 222024: 112025: 302026 (partial year): 42
2007high 42 (2026) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OWB

14,008in 2025

2007: 12011: 12012: 12013: 272014: 1032015: 2,1342016: 4,0742017: 1,6042018: 1,4492019: 1,5582020: 1,5812021: 1,9812022: 2,9322023: 7,6042024: 7,9422025: 14,008
2007high 14,008 (2025) · low 0 (2008)2025

MAUDE reports naming product code OWB, 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
200735201
2008413510
200999900
201076600
201167901
201263701
2013111191027
2014151589103
20151166352,134
201616103134,074
20172076131,604
2018235461,449
2019917471,558
2020165381,581
20212460311,981
20222190242,932
202312152227,604
202413126117,942
2025221483014,008
20261522142—

What is it indicated for?

The Trinias is an angiographic X-ray system, which is used for diagnostic imaging and interventional procedures. The Trinias is intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K221922: Trinias.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K221922

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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