510(k) · Cleared
ClearedAesculap Trelon Nonabsorbable Multifilament Polyamide Surgical Suture
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aesculap, Inc. · GAR Suture, Nonabsorbable, Synthetic, Polyamide
Cleared on Mar 28, 2006 as substantially equivalent to K990090 (Aesculap, Inc., 1999) after a 28-day review. Its family tree reaches back 1 generation to 1999.
- Decided
- Mar 28, 2006
- Review
- 28 days
- Class
- Class II
- Product code
- GAR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K990090 (1999). No later device cites it as a predicate yet.
- Root · 1 generation backK990090 Dafilon Nonabsorbable Polyamide Surgical SutureAesculap, Inc. · 1999 · Recalled
- This deviceK060528 Aesculap Trelon Nonabsorbable Multifilament Polyamide Surgical SutureAesculap, Inc. · 2006
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K990090 | Dafilon Nonabsorbable Polyamide Surgical Suture | Aesculap, Inc. | 1999 | 1 |
| 0 (this device) | K060528 | Aesculap Trelon Nonabsorbable Multifilament Polyamide Surgical Suture | Aesculap, Inc. | 2006 | — |
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 K261484 Tissue Approximation Systemscore 11.8 · 2 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 |
|---|---|---|---|
| * | K990090 | Dafilon Nonabsorbable Polyamide Surgical SutureSummary page 1…p®, Inc. believes that the Trelon® sutures described here are substantially equivalent to the Dafilon® sutures previously cleared in the Aesculap Premarket Notification #K990090. DEVICE DESCRIPTION The Trelon® sutures are a polyamide (Nylon) multifilament suture that is available in common sizes and lengt… | 1999 |
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?
- Its one ancestor has a recall.
- 1 other device also cites its predicate K990090.
How does its category compare?
All GAR devicesGAR Suture, Nonabsorbable, Synthetic, Polyamide: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GAR
1in 2023
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
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GAR
823in 2025
MAUDE reports naming product code GAR, 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 | 18 |
| 2008 | 1 | — | 1 | 14 |
| 2009 | 0 | — | 0 | 12 |
| 2010 | 0 | — | 0 | 39 |
| 2011 | 0 | — | 1 | 8 |
| 2012 | 0 | — | 0 | 5 |
| 2013 | 1 | — | 0 | 42 |
| 2014 | 0 | — | 0 | 103 |
| 2015 | 1 | — | 0 | 86 |
| 2016 | 1 | — | 0 | 124 |
| 2017 | 1 | — | 0 | 180 |
| 2018 | 0 | — | 0 | 541 |
| 2019 | 0 | — | 0 | 518 |
| 2020 | 1 | — | 0 | 384 |
| 2021 | 1 | — | 0 | 532 |
| 2022 | 1 | — | 0 | 549 |
| 2023 | 1 | — | 1 | 607 |
| 2024 | 0 | — | 0 | 668 |
| 2025 | 0 | — | 0 | 823 |
| 2026 | 1 | — | 1 | — |
What is it indicated for?
Trelon® sutures are intended for use in general and soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic, and neurological procedures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K060528 · printed Nov 4, 2026
Cite this page
510(k) Report. “K060528: Aesculap Trelon Nonabsorbable Multifilament Polyamide Surgical Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K060528
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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