510(k) Report

510(k) · Cleared

Cleared

JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps Valve

K210625510(k) TraditionalCleared Sep 10, 2021192-day reviewClass II21 CFR 876.1500

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

Fujifilm Medwork GmbH · ODC Endoscope Channel Accessory

Cleared on Sep 10, 2021 as substantially equivalent to K102581 (Byrne Medical, Inc., 2010) and 2 other predicates after a 192-day review. Its family tree reaches back 2 generations to 2000. 1 later device descends from it.

Decided
Sep 10, 2021
Review
192 days
Class
Class II
Product code
ODC
Recalls
None
Predicates
3

Its longest line of descent runs back 2 generations to K001241 (2000). 4 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2009: 1 other ancestor2022: 1 descendant clearedK001241 · Evis Exera Colonovideoscope CF-Q160 AL/I and PCF-160 AL/I · The Olympus Optical Co. · 2000 · recalledK102409 · Defendo Disposable Air/Water Valve Model 100304 · Byrne Medical, Inc. · 2010200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors 1 generation forward: 1 descendant K102409 · Defendo Disposable Air/Water Valve Model 100304 · Byrne Medical, Inc. · 2010K001241 · Evis Exera Colonovideoscope CF-Q160 AL/I and PCF-160 AL/I · The Olympus Optical Co. · 2000 · recalled0
  1. Root · 2 generations backK001241 Evis Exera Colonovideoscope CF-Q160 AL/I and PCF-160 AL/IThe Olympus Optical Co. · 2000 · Recalled
  2. 1 generation backK102409 Defendo Disposable Air/Water Valve Model 100304Byrne Medical, Inc. · 2010
  3. This deviceK210625 JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps ValveFujifilm Medwork GmbH · 2021
  4. Descendant · cites it directly · 0 of its ownK221264 FROG Forceps Valve (VAL1-F1-100)Fujifilm Medwork GmbH · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K221264FROG Forceps Valve (VAL1-F1-100)Fujifilm Medwork GmbH · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K001241Evis Exera Colonovideoscope CF-Q160 AL/I and PCF-160 AL/IThe Olympus Optical Co.20001
−1K102409Defendo Disposable Air/Water Valve Model 100304Byrne Medical, Inc.2010—
0 (this device)K210625JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps ValveFujifilm Medwork GmbH2021—
+1K221264FROG Forceps Valve (VAL1-F1-100)Fujifilm Medwork GmbH2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200910
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K210625, 2000–2022Source: 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 ODC? 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 ODC device

  1. #1 K232329 Defendo Fujifilm 700 Single Use Biopsy Valve…score 14.0 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (3)

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
*K102581Defendo Disposable Suction Valve Model 100305
Summary page 4
…nd accessories Device Panel: Gastroentereology/Urology Product Codes: ODC, FDF Predicate Devices: • DEFENDO Disposable Suction Valve Model 100305 (K102581) • DEFENDO Disposable Air/Water Valve Model 100304 (K102409) • DEFENDO Disposable Biopsy Valve Model 100301 (K090851)…
Byrne Medical, Inc.2010—
*K102409Defendo Disposable Air/Water Valve Model 100304
Summary page 4
…Product Codes: ODC, FDF Predicate Devices: • DEFENDO Disposable Suction Valve Model 100305 (K102581) • DEFENDO Disposable Air/Water Valve Model 100304 (K102409) • DEFENDO Disposable Biopsy Valve Model 100301 (K090851) Intended Use / Indications for Use The JAZZ Disposable Valve Kit…
Byrne Medical, Inc.2010—
*K090851Defendo (TM) Biopsy Valve for Olympus (R) and Fujinon (R) Endoscopes, Model 100301…
Summary page 4
…NDO Disposable Suction Valve Model 100305 (K102581) • DEFENDO Disposable Air/Water Valve Model 100304 (K102409) • DEFENDO Disposable Biopsy Valve Model 100301 (K090851) Intended Use / Indications for Use The JAZZ Disposable Valve Kit is comprised of the JAZZ Suction Valve, JAZZ Air/Water Valve,…
Byrne Medical, Inc.2009—

Also cleared against K102581: 8 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K221264FROG Forceps Valve (VAL1-F1-100)Fujifilm Medwork GmbH20220

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 21 years and passes through 3 companies; a new generation was cleared every 10.9 years on median.
  • 1 of the 4 ancestors has a recall of any class.
  • Of its descendants, K221264 (Fujifilm Medwork GmbH, 2022) has gone furthest, with 0 descendants of its own.
  • 8 other devices also cite its predicate K102581.

How does its category compare?

All ODC devices

ODC Endoscope Channel Accessory: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · ODC

6in 2025

2008: 32009: 12010: 42011: 42012: 22015: 22016: 12017: 12018: 22019: 42020: 42021: 62022: 82023: 72024: 82025: 62026 (partial year): 1
2007high 8 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODC

106in 2025

2008: 83 days median2010: 67 days median2011: 143 days median2019: 55 days median2020: 128 days median2021: 181 days median2022: 118 days median2023: 126 days median2024: 95 days median2025: 106 days median
2007high 181 (2021) · low 55 (2019)2026

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

Recalls per year · ODC

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

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

Adverse event reports per year · ODC

91in 2025

2012: 12013: 12014: 22015: 32016: 82017: 122018: 172019: 402020: 542021: 522022: 372023: 432024: 1002025: 91
2007high 100 (2024) · low 0 (2007)2025

MAUDE reports naming product code ODC, 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
20070—00
200838300
20091—00
201046700
2011414300
20122—01
20130—01
20140—02
20152—03
20161—08
20171—012
20182—017
2019455040
20204128054
20216181052
20228118037
20237126043
20248950100
20256106091
20261—1—

What is it indicated for?

The JAZZ Disposable Valve Kit is comprised of the JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps Valve.

The JAZZ Suction Valve is intended to control the suction function (aspiration of air and fluids) of a FUJIFILM gastrointestinal endoscope during endoscopy procedures.

The JAZZ Air/Water Valve is intended to control air of a FUJIFILM gastrointestinal endoscope for insufflations and water delivery (for distal lens cleaning) during endoscopy procedures.

The JAZZ Forceps Valve is intended to facilitate passage of an endotherapy device, to prevent a leak or backflow of air and/or fluids, and to enable the suction function of a FUJIFILM gastrointestinal endoscope.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K210625: JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps Valve.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K210625

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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