510(k) · Cleared
ClearedPremicron Nonabsorbable Pet Surgical Suture
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aesculap, Inc. · GAT Suture, Nonabsorbable, Synthetic, Polyethylene
Cleared on Sep 19, 2001 after a 68-day review. The FDA summary names its predicate without a number. 6 later devices descend from it.
- Decided
- Sep 19, 2001
- Review
- 68 days
- Class
- Class II
- Product code
- GAT
- Recalls
- None
- Predicates
- 0
6 later devices descend from it, 1 citing it directly.
- This deviceK012201 Premicron Nonabsorbable Pet Surgical SutureAesculap, Inc. · 2001
- Descendant · cites it directly · 5 of its ownK133890 Aesculap Optilene Nonabsorbable SutureAesculap, Inc. · 2014
- Descendant · 2 generations on · 3 of its ownK151165 Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureAesculap, Inc. · 2016
- Descendant · 3 generations on · 1 of its ownK192420 Crownjun Nylon SutureKono Seisakusho Co., Ltd. · 2020
- Descendant · 4 generations on · 0 of its ownK221280 VessealLydus Medical, Ltd. · 2022
- Descendant · 3 generations on · 0 of its ownK212603 Non Absorbable Surgical Nylon SutureShandong Haidike Medical Product Co., Ltd. · 2021
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K133890Aesculap Optilene Nonabsorbable SutureAesculap, Inc. · 2014 · cites it directly5descendants
- K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureAesculap, Inc. · 2016 · 2 generations on3descendants
- K192420Crownjun Nylon SutureKono Seisakusho Co., Ltd. · 2020 · 3 generations on1descendant
- K221280VessealLydus Medical, Ltd. · 2022 · 4 generations on0descendants
- K212603Non Absorbable Surgical Nylon SutureShandong Haidike Medical Product Co., Ltd. · 2021 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K012201 | Premicron Nonabsorbable Pet Surgical Suture | Aesculap, Inc. | 2001 | — |
| +1 | K133890 | Aesculap Optilene Nonabsorbable Suture | Aesculap, Inc. | 2014 | — |
| +2 | K151165 | Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture | Aesculap, Inc. | 2016 | — |
| +3 | K192420 | Crownjun Nylon Suture | Kono Seisakusho Co., Ltd. | 2020 | — |
| +4 | K221280 | Vesseal | Lydus Medical, Ltd. | 2022 | — |
| +3 | K212603 | Non Absorbable Surgical Nylon Suture | Shandong Haidike Medical Product Co., Ltd. | 2021 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2018 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
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 GAT? 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 GAT device
- #1 K230311 HyperSuturescore 20.2 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | — | SURGIDAC® Nonabsorbable Surgical Suture (U. S. Surgical Corp.) Named without a submission number | |
| * | — | ETHIBOND® Nonabsorbable Surgical Suture (Ethicon, Inc.) Named without a submission number | |
| * | — | TI-CRON® Nonabsorbable Surgical Suture (Sherwood Davis & Geck) Named without a submission number | |
| * | — | Synthofil® Nonabsorbable Surgical Suture (AESCULAP®) Named without a submission number |
What descends from it? (6)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K133890 | Aesculap Optilene Nonabsorbable Suture | 2014 | 5 |
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?
- Of its descendants, K133890 (Aesculap, Inc., 2014) has gone furthest, with 5 descendants of its own.
How does its category compare?
All GAT devicesGAT Suture, Nonabsorbable, Synthetic, Polyethylene: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GAT
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GAT
30in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GAT
1in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GAT
2,956in 2025
MAUDE reports naming product code GAT, 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 | 6 | 40 | 1 | 15 |
| 2008 | 4 | 93 | 0 | 15 |
| 2009 | 9 | 57 | 0 | 55 |
| 2010 | 11 | 27 | 3 | 79 |
| 2011 | 1 | — | 1 | 97 |
| 2012 | 6 | 61 | 0 | 253 |
| 2013 | 4 | 123 | 0 | 210 |
| 2014 | 4 | 45 | 0 | 165 |
| 2015 | 7 | 125 | 0 | 626 |
| 2016 | 10 | 139 | 0 | 688 |
| 2017 | 6 | 57 | 0 | 1,104 |
| 2018 | 6 | 95 | 0 | 1,453 |
| 2019 | 4 | 79 | 0 | 1,251 |
| 2020 | 5 | 201 | 0 | 1,220 |
| 2021 | 4 | 92 | 0 | 1,643 |
| 2022 | 5 | 109 | 0 | 1,419 |
| 2023 | 8 | 220 | 0 | 2,038 |
| 2024 | 3 | 140 | 0 | 2,597 |
| 2025 | 5 | 30 | 0 | 2,956 |
| 2026 | 5 | 83 | 0 | — |
What is it indicated for?
PremiCron® Nonabsorbable Surgical Suture is indicated for use in
general soft tissue approximation and/or ligation, including use in
cardiovascular and vascular, ophthalmic and neurological procedures.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K012201 · printed Nov 3, 2026
Cite this page
510(k) Report. “K012201: Premicron Nonabsorbable Pet Surgical Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K012201
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026