510(k) Report

510(k) · Cleared

Cleared

Crownjun Nylon Suture

K192420510(k) TraditionalCleared May 29, 2020268-day reviewClass II21 CFR 878.5020

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

Kono Seisakusho Co., Ltd. · GAR Suture, Nonabsorbable, Synthetic, Polyamide

Cleared on May 29, 2020 as substantially equivalent to K151165 (Aesculap, Inc., 2016) after a 268-day review. Its family tree reaches back 4 generations to 1996. 1 later device descends from it.

Decided
May 29, 2020
Review
268 days
Class
Class II
Product code
GAR
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K954808 (1996). 8 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK954808 Ussc Polyproplene SutureUnited States Surgical, A Division of Tyco Healthc · 1996 · Recalled
  2. 3 generations backK050947 Modification to: Modified Uss Polypropylene SutureUnited States Surgical, A Division of Tyco Healthc · 2005 · Recalled
  3. 2 generations backK133890 Aesculap Optilene Nonabsorbable SutureAesculap, Inc. · 2014
  4. 1 generation backK151165 Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureAesculap, Inc. · 2016
  5. This deviceK192420 Crownjun Nylon SutureKono Seisakusho Co., Ltd. · 2020
  6. Descendant · cites it directly · 0 of its ownK221280 VessealLydus Medical, Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K221280VessealLydus Medical, Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K954808Ussc Polyproplene SutureUnited States Surgical, A Division of Tyco Healthc19961
−3K050947Modification to: Modified Uss Polypropylene SutureUnited States Surgical, A Division of Tyco Healthc20052
−2K133890Aesculap Optilene Nonabsorbable SutureAesculap, Inc.2014—
−1K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureAesculap, Inc.2016—
0 (this device)K192420Crownjun Nylon SutureKono Seisakusho Co., Ltd.2020—
+1K221280VessealLydus Medical, Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
199910
200120

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K192420, 1996–2022Source: 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 GAR? 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 GAR device

  1. #1 K261484 Tissue Approximation Systemscore 11.7 · 2 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? (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
*K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture
Summary page 4
…I Classification: 21 CFR 878.5020 Nonabsorbable Polyamide Surgical Suture Product Code: GAR Predicate Devices: K151165, AESCULAP, INC. Dafilon Nonabsorbable Polyamide Surgical Suture. Device Description: The CROWNJUN Nylon Suture is a s…
Aesculap, Inc.2016—

Also cleared against K151165: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K221280VessealLydus Medical, Ltd.20220

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 9.1 years on median.
  • 3 of the 8 ancestors have a recall of any class.
  • Of its descendants, K221280 (Lydus Medical, Ltd., 2022) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K151165.

How does its category compare?

All GAR devices

GAR Suture, Nonabsorbable, Synthetic, Polyamide: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · GAR

1in 2023

2008: 12013: 12015: 12016: 12017: 12020: 12021: 12022: 12023: 12026 (partial year): 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAR

Too few GAR 510(k)s in any year since 2007 to give a median.

Recalls per year · GAR

1in 2023

2008: 12011: 12023: 12026 (partial year): 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · GAR

823in 2025

2007: 182008: 142009: 122010: 392011: 82012: 52013: 422014: 1032015: 862016: 1242017: 1802018: 5412019: 5182020: 3842021: 5322022: 5492023: 6072024: 6682025: 823
2007high 823 (2025) · low 5 (2012)2025

MAUDE reports naming product code GAR, 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—018
20081—114
20090—012
20100—039
20110—18
20120—05
20131—042
20140—0103
20151—086
20161—0124
20171—0180
20180—0541
20190—0518
20201—0384
20211—0532
20221—0549
20231—1607
20240—0668
20250—0823
20261—1—

What is it indicated for?

CROWNJUN Nylon Suture is intended to join the edges of soft-tissue wound or incision to ligate soft tissues.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192420: Crownjun Nylon Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192420

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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