510(k) · Cleared
ClearedAdvincula Delineator Uterine Manipulator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
CooperSurgical, Inc. · HEW Culdoscope (And Accessories)
Cleared on May 21, 2020 as substantially equivalent to K180429 (CooperSurgical, Inc., 2018) after a 28-day review. Its family tree reaches back 3 generations to 1996.
- Decided
- May 21, 2020
- Review
- 28 days
- Class
- Class II
- Product code
- HEW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K954311 (1996). No later device cites it as a predicate yet.
- Root · 3 generations backK954311 Koh Colpotomizer SystemCooperSurgical, Inc. · 1996 · Recalled
- 2 generations backK143650 CooperSurgical Advincula Delineator Uterine ManipulatorCooperSurgical, Inc. · 2015
- 1 generation backK180429 Advincula Delineator Uterine ManipulatorCooperSurgical, Inc. · 2018 · Recalled
- This deviceK201086 Advincula Delineator Uterine ManipulatorCooperSurgical, Inc. · 2020
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K954311 | Koh Colpotomizer System | CooperSurgical, Inc. | 1996 | 2 |
| −2 | K143650 | CooperSurgical Advincula Delineator Uterine Manipulator | CooperSurgical, Inc. | 2015 | — |
| −1 | K180429 | Advincula Delineator Uterine Manipulator | CooperSurgical, Inc. | 2018 | 2 |
| 0 (this device) | K201086 | Advincula Delineator Uterine Manipulator | CooperSurgical, Inc. | 2020 | — |
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 HEW? 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 HEW device
- #1 K243152 GelPOINT V-Path Transvaginal Access Platform…score 11.0 · 4 generations · no Class I recall
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 |
|---|---|---|---|
| * | K180429 | Advincula Delineator Uterine ManipulatorSummary page 4…Class II Product Code: HEW Product Code Name: Culdoscope (and Accessories) PREDICATE DEVICE INFORMATION Advincula Delineator™ Uterine Manipulator (K180429). The predicate device has not been subject to a design-related recall. DEVICE DESCRIPTION The Advincula Delineator Uterine Man… | 2018 |
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 1 company; a new generation was cleared every 2.6 years on median.
- 2 of the 3 ancestors have a recall of any class.
How does its category compare?
All HEW devicesHEW Culdoscope (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · HEW
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HEW
Too few HEW 510(k)s in any year since 2007 to give a median.
Recalls per year · HEW
1in 2018
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HEW
20in 2025
MAUDE reports naming product code HEW, 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 | 1 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 0 | — | 0 | 4 |
| 2010 | 0 | — | 0 | 3 |
| 2011 | 1 | — | 0 | 3 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 0 | — | 0 | 3 |
| 2014 | 0 | — | 0 | 2 |
| 2015 | 2 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 9 |
| 2017 | 0 | — | 0 | 15 |
| 2018 | 1 | — | 1 | 14 |
| 2019 | 1 | — | 0 | 29 |
| 2020 | 1 | — | 0 | 35 |
| 2021 | 0 | — | 0 | 14 |
| 2022 | 0 | — | 0 | 23 |
| 2023 | 0 | — | 0 | 18 |
| 2024 | 0 | — | 0 | 32 |
| 2025 | 1 | — | 0 | 20 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The CooperSurgical Advincula Delineator™ Uterine Manipulator is indicated to provide delineation of the vaginal fornices and maintain pneumoperitoneum as a uterine manipulator during Total Laparoscopic Hysterectomy, Laparoscopic Assisted Vaginal Hysterectomy and/or Laparoscopic Supra-Cervical Hysterectomy.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K201086 · printed Nov 6, 2026
Cite this page
510(k) Report. “K201086: Advincula Delineator Uterine Manipulator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201086
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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