510(k) Report

510(k) · Cleared

Cleared

JFil Ureteral Stents, JFil Ureteral Stents ECO KIT

K212868510(k) TraditionalCleared Jan 26, 2022139-day reviewClass II21 CFR 876.4620

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

Rocamed Sam · FAD Stent, Ureteral

Cleared on Jan 26, 2022 as substantially equivalent to K030503 (Boston Scientific Corp, 2003) and 1 other predicate after a 139-day review. Its family tree reaches back 6 generations to 1991.

Decided
Jan 26, 2022
Review
139 days
Class
Class II
Product code
FAD
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K903345 (1991). 10 ancestors in all, the oldest K905289 (1991). No later device cites it as a predicate yet.

  1. Root · 6 generations backK903345 Bard (R) Lubricious - Coated Ureteral Stent SutureC.R. Bard, Inc. · 1991
  2. 5 generations backK983498 Bard Inlay Lubricious Double Pigtail Ureteral Stent with Suture…C.R. Bard, Inc. · 1998 · Recalled
  3. 4 generations backK022447 Bard ER Ureteral Stent with SutureC.R. Bard, Inc. · 2003
  4. 3 generations backK043193 Bard Inlayoptima Ureteral Stent with SutureC.R. Bard, Inc. · 2004 · Recalled
  5. 2 generations backK151051 Universa Soft Ureteral Stents and Stent SetsCook Incorporated · 2016 · Recalled
  6. 1 generation backK173734 RocaJJ Soft StentsPromepla Sam · 2018
  7. This deviceK212868 JFil Ureteral Stents, JFil Ureteral Stents ECO KITRocamed Sam · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K903345Bard (R) Lubricious - Coated Ureteral Stent SutureC.R. Bard, Inc.1991—
−5K983498Bard Inlay Lubricious Double Pigtail Ureteral Stent with Suture (Hereinafter…C.R. Bard, Inc.19982
−4K022447Bard ER Ureteral Stent with SutureC.R. Bard, Inc.2003—
−3K043193Bard Inlayoptima Ureteral Stent with SutureC.R. Bard, Inc.20046
−2K151051Universa Soft Ureteral Stents and Stent SetsCook Incorporated20162
−1K173734RocaJJ Soft StentsPromepla Sam2018—
0 (this device)K212868JFil Ureteral Stents, JFil Ureteral Stents ECO KITRocamed Sam2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199610
200110
200310
FIG. 1 — Lineage of K212868, 1991–2022Source: 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 FAD? 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 FAD device

  1. #1 K251890 Disposable Ureteral Stentsscore 12.4 · 6 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? (2)

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
*K030503Modification to Contour Polaris Ureteral Stent
Summary page 5
…II Review Panel Gastroenterology/Urology Product Code FAD 3. Predicate Devices 510(k) number K030503 K173734 Owner Boston Scientific Corp. Promepla SAM Tra…
Boston Scientific Corp2003—
*K173734RocaJJ Soft Stents
Summary page 5
…Gastroenterology/Urology Product Code FAD 3. Predicate Devices 510(k) number K030503 K173734 Owner Boston Scientific Corp. Promepla SAM Trade name of the Device Polaris Lo…
Promepla Sam2018—

What descends from it?

No later submission names this one as a predicate yet.

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 31 years and passes through 4 companies; a new generation was cleared every 4.1 years on median.
  • 5 of the 10 ancestors have a recall of any class.

How does its category compare?

All FAD devices

FAD Stent, Ureteral: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · FAD

4in 2025

2007: 12008: 12010: 12014: 12016: 42017: 82018: 92019: 52020: 12021: 22022: 52024: 12025: 42026 (partial year): 1
2007high 9 (2018) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FAD

186in 2025

2016: 143 days median2017: 266 days median2018: 258 days median2019: 263 days median2022: 143 days median2025: 186 days median
2007high 266 (2017) · low 143 (2016)2026

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

Recalls per year · FAD

4in 2025

2007: 12008: 222009: 22010: 12016: 42019: 62020: 22021: 12022: 92025: 4
2007high 22 (2008) · low 0 (2011)2026

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

Adverse event reports per year · FAD

634in 2025

2007: 432008: 762009: 1232010: 782011: 952012: 1312013: 822014: 782015: 1302016: 1822017: 2652018: 2772019: 2612020: 3522021: 5312022: 5592023: 6912024: 6032025: 634
2007high 691 (2023) · low 43 (2007)2025

MAUDE reports naming product code FAD, 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
20071—143
20081—2276
20090—2123
20101—178
20110—095
20120—0131
20130—082
20141—078
20150—0130
201641434182
201782660265
201892580277
201952636261
20201—2352
20212—1531
202251439559
20230—0691
20241—0603
202541864634
20261—0—

What is it indicated for?

The JFil® Ureteral Stents are used for temporary internal drainage of the ureteropelvic junction.

The stents may be placed using endoscopic techniques.

The stents are not intended as permanent indwelling devices, it is recommended that the indwelling time does not exceed 14 days.

Target population: adults only (greater than 21 years of age).

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. “K212868: JFil Ureteral Stents, JFil Ureteral Stents ECO KIT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K212868

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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