510(k) · Cleared
ClearedAccumesh Deployment System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Covidien, LLC · ORQ Mesh, Surgical, Deployer
Cleared on Apr 5, 2013 as substantially equivalent to K101218 (Polytouch Medical, Ltd., 2010) and 2 other predicates after a 15-day review. Its family tree reaches back 4 generations to 2010.
- Decided
- Apr 5, 2013
- Review
- 15 days
- Class
- Class II
- Product code
- ORQ
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 4 generations to K101218 (2010). No later device cites it as a predicate yet.
- Root · 4 generations backK101218 PatchassistPolytouch Medical, Ltd. · 2010
- 3 generations backK103269 Patchassist LargePolytouch Medical, Ltd. · 2010
- 2 generations backK121139 Accumesh Deployment SystemCovidien, LLC · 2012
- 1 generation backK123066 Accumesh Deployment SystemCovidien, LLC · 2012
- This deviceK130782 Accumesh Deployment SystemCovidien, LLC · 2013
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K101218 | Patchassist | Polytouch Medical, Ltd. | 2010 | — |
| −3 | K103269 | Patchassist Large | Polytouch Medical, Ltd. | 2010 | — |
| −2 | K121139 | Accumesh Deployment System | Covidien, LLC | 2012 | — |
| −1 | K123066 | Accumesh Deployment System | Covidien, LLC | 2012 | — |
| 0 (this device) | K130782 | Accumesh Deployment System | Covidien, LLC | 2013 | — |
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 ORQ? 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 ORQ device
- #1 K250395 BioBrace ® RC Delivery Systemscore 12.7 · 13 generations · no Class I recall
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K101218 | PatchassistSummary page 1…o which equivalence is claimed: o Accumesh Positioning System (510k cleared as the PatchAssist device - K101218 o Accumesh Positioning System PatchAssist Large (510k cleared a… | 2010 |
| * | K103269 | Patchassist LargeSummary page 2…ame, itself, has not changed and is previously cleared in the AccuMesh (PatchAssist) device (K101218, K103269, and K123066) 510(k)s. Accumesh is intended to be used to facilitate the… | 2010 |
| * | K123066 | Accumesh Deployment SystemSummary page 1…em PatchAssist Large (510k cleared as the PatchAssist device - KI103269 o AccuMesh Positioning System - K123066 14 Covidien… | 2012 |
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 3 years and passes through 2 companies; a new generation was cleared every 6 months on median.
- None of the 4 ancestors has a recall.
- 3 other devices also cite its predicate K101218.
How does its category compare?
All ORQ devicesORQ Mesh, Surgical, Deployer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · ORQ
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ORQ
Too few ORQ 510(k)s in any year since 2007 to give a median.
Recalls per year · ORQ
No recall names ORQ since 2007.
Adverse event reports per year · ORQ
11in 2025
MAUDE reports naming product code ORQ, 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 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 2 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 1 |
| 2015 | 0 | — | 0 | 1 |
| 2016 | 0 | — | 0 | 10 |
| 2017 | 0 | — | 0 | 10 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 5 |
| 2022 | 0 | — | 0 | 2 |
| 2023 | 0 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 11 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The AccuMesh Positioning System is intended to be used to facilitate the delivery of soft tissue prosthetics during the laparoscopic repair of soft tissue defects (e.g. hernia repair).
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K130782 · printed Nov 4, 2026
Cite this page
510(k) Report. “K130782: Accumesh Deployment System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K130782
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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