510(k) · Cleared
ClearedStitchKit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Origami Surgical · NBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene
Cleared on Jul 12, 2019 as substantially equivalent to K123811 (Origami Surgical, LLC, 2013) and 1 other predicate after a 58-day review. Its family tree reaches back 3 generations to 1995.
- Decided
- Jul 12, 2019
- Review
- 58 days
- Class
- Class II
- Product code
- NBY
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 3 generations to K954853 (1995). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 3 generations backK954853 Auto Suture Suture ClosureUnited States Surgical, A Division of Tyco Healthc · 1995
- 2 generations backK981531 Suture Placement Device and AccessoriesLsi Solutions · 1998
- 1 generation backK123811 StitchkitOrigami Surgical, LLC · 2013
- This deviceK191317 StitchKitOrigami Surgical · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K954853 | Auto Suture Suture Closure | United States Surgical, A Division of Tyco Healthc | 1995 | — |
| −2 | K981531 | Suture Placement Device and Accessories | Lsi Solutions | 1998 | — |
| −1 | K123811 | Stitchkit | Origami Surgical, LLC | 2013 | — |
| 0 (this device) | K191317 | StitchKit | Origami Surgical | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 1 | 0 |
| 2014 | 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 NBY? 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 NBY device
- #1 K231277 TissueStatscore 6.9 · 3 generations · no Class I recall
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K123811 | StitchkitSummary page 4…Polytetrafluoroethylene Surgical Suture. Product code NBY; Secondary Codes: GCJ and NAY Predicate Devices: K123811 StitchKit® Suture Delivery Canister K140415 Riverpoint Medical Monotex® PTFE Suture Device Descri… | 2013 |
| * | K140415 | MonotexSummary page 4…Product code NBY; Secondary Codes: GCJ and NAY Predicate Devices: K123811 StitchKit® Suture Delivery Canister K140415 Riverpoint Medical Monotex® PTFE Suture Device Description: StitchKit® is a suture delivery canister which facilitates endoscop… | 2014 |
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 24 years and passes through 4 companies; a new generation was cleared every 5.8 years on median.
- None of the 5 ancestors has a recall.
- 2 other devices also cite its predicate K123811.
How does its category compare?
All NBY devicesNBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · NBY
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · NBY
58in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NBY
No recall names NBY since 2007.
Adverse event reports per year · NBY
1in 2025
MAUDE reports naming product code NBY, 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 | 1 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 3 | 161 | 0 | 0 |
| 2018 | 4 | 99 | 0 | 0 |
| 2019 | 3 | 58 | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 0 | — | 0 | 4 |
| 2023 | 1 | — | 0 | 5 |
| 2024 | 0 | — | 0 | 3 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The StitchKit® device facilitates minimally invasive robotic surgery by transporting suture to the operative field and removing used needles after suturing.
Monotex® PTFE surgical suture is indicated for use in general soft tissue approximation and/or ligation, including cardiovascular, dental, general surgical procedures and repair of the dura mater. Monotex® PTFE sutures are not indicated for use in microsurgery, ophthalmic procedures, or peripheral neural tissues. Monotex® PTFE suture is provided sterile as a single use device.
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/K191317 · printed Nov 6, 2026
Cite this page
510(k) Report. “K191317: StitchKit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191317
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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