510(k) · Cleared
ClearedSupris Retropubic Sling System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Coloplast A/S · OTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
Cleared on Jun 24, 2011 as substantially equivalent to K053296 (Mentor Corporation, 2005) after a 53-day review. Its family tree reaches back 6 generations to 2001. 1 later device descends from it.
- Decided
- Jun 24, 2011
- Review
- 53 days
- Class
- Class II
- Product code
- OTN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K011251 (2001). 9 ancestors in all, the oldest K974098 (1998). 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK011251 Sparc Sling SystemAmerican Medical Systems, Inc. · 2001
- 5 generations backK013355 Sparc Sling SystemAmerican Medical Systems, Inc. · 2001
- 4 generations backK031767 Mentor Obtape Trans-Obturator TapeMentor Corp. · 2003
- 3 generations backK042851 Mentor Obtape Trans-Obturator Surgical KitMentor Corp. · 2004
- 2 generations backK050148 Mentor Aris Trans-Obturator Tape and Surgical KitMentor Corporation · 2005
- 1 generation backK053296 Mentor Aris Suprapubic Surgical KitMentor Corporation · 2005
- This deviceK111233 Supris Retropubic Sling SystemColoplast A/S · 2011
- Descendant · cites it directly · 0 of its ownK242473 Altis Single Incision Sling System (519650); Aris Transobturator…Coloplast Corp. · 2024
Most influential descendants
Showing 1 of 1 · See all- K242473Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551)…Coloplast Corp. · 2024 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K011251 | Sparc Sling System | American Medical Systems, Inc. | 2001 | — |
| −5 | K013355 | Sparc Sling System | American Medical Systems, Inc. | 2001 | — |
| −4 | K031767 | Mentor Obtape Trans-Obturator Tape | Mentor Corp. | 2003 | — |
| −3 | K042851 | Mentor Obtape Trans-Obturator Surgical Kit | Mentor Corp. | 2004 | — |
| −2 | K050148 | Mentor Aris Trans-Obturator Tape and Surgical Kit | Mentor Corporation | 2005 | — |
| −1 | K053296 | Mentor Aris Suprapubic Surgical Kit | Mentor Corporation | 2005 | — |
| 0 (this device) | K111233 | Supris Retropubic Sling System | Coloplast A/S | 2011 | — |
| +1 | K242473 | Altis Single Incision Sling System (519650); Aris Transobturator Sling System… | Coloplast Corp. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2002 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 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 OTN? 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 OTN device
- #1 K231549 Advantage Ultra System, Advantage Fit Ultra…score 6.8 · 5 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 |
|---|---|---|---|
| * | K053296 | Mentor Aris Suprapubic Surgical KitSummary page 1…21 CFR §878.3300 Product Code: OTN, FTL Predicate Devices: Mentor ArisTM Suprapubic Surgical Kit K053296 Description of Device: The Supris Retropubic Sling System is a permanent, synthetic sub-urethral sling that is provided with dis… | 2005 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K242473 | Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551)… | 2024 | 0 |
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 10 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
- None of the 9 ancestors has a recall.
- Of its descendants, K242473 (Coloplast Corp., 2024) has gone furthest, with 0 descendants of its own.
How does its category compare?
All OTN devicesOTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · OTN
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · OTN
89in 2021
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OTN
1in 2014
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OTN
458in 2025
MAUDE reports naming product code OTN, 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 | 2 | — | 0 | 0 |
| 2008 | 3 | 100 | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 5 | 25 | 0 | 1 |
| 2011 | 4 | 56 | 0 | 25 |
| 2012 | 1 | — | 0 | 874 |
| 2013 | 5 | 86 | 0 | 19,084 |
| 2014 | 1 | — | 1 | 2,063 |
| 2015 | 0 | — | 0 | 3,904 |
| 2016 | 0 | — | 0 | 1,902 |
| 2017 | 1 | — | 0 | 676 |
| 2018 | 0 | — | 0 | 737 |
| 2019 | 1 | — | 0 | 2,457 |
| 2020 | 1 | — | 0 | 1,003 |
| 2021 | 3 | 89 | 0 | 2,606 |
| 2022 | 2 | — | 0 | 809 |
| 2023 | 1 | — | 0 | 1,076 |
| 2024 | 0 | — | 0 | 822 |
| 2025 | 0 | — | 0 | 458 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Supris Retropubic Sling System is an implantable, sub-urethral, support tape indicated for the surgical treatment of female stress urinary incontinence (SUT), resulting from urethral hypermobility and/or intrinsic sphincter deficiency. The sling is plaiced retropubically using two disposable introducers using either a "top down" or "bottom up" surgical approach
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111233 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111233: Supris Retropubic Sling System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111233
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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