510(k) · Cleared
Recalled · Class II · 2019Revive Reusable Bladder Support
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Rinovum Subsidiary 2, LLC · HHW Pessary, Vaginal
Cleared on Jan 25, 2019 as substantially equivalent to K151413 (Procter & Gamble, 2015) after a 42-day review. Its family tree reaches back 4 generations to 1995. It has been recalled once.
- Decided
- Jan 25, 2019
- Review
- 42 days
- Class
- Class II
- Product code
- HHW
- Recalls
- 1
- Predicates
- 1
Its longest line of descent runs back 4 generations to K930618 (1995). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 4 generations backK930618 Vaginal Continence DeviceJohnson & Johnson Medical, Inc. · 1995
- 3 generations backK060526 TIPIContipi, Ltd. · 2006
- 2 generations backK131198 Tipi OtcContipi, Ltd. · 2013
- 1 generation backK151413 Always/Tampax bladder supportsProcter & Gamble · 2015
- This deviceK183468 Revive Reusable Bladder SupportRinovum Subsidiary 2, LLC · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K930618 | Vaginal Continence Device | Johnson & Johnson Medical, Inc. | 1995 | — |
| −3 | K060526 | TIPI | Contipi, Ltd. | 2006 | — |
| −2 | K131198 | Tipi Otc | Contipi, Ltd. | 2013 | — |
| −1 | K151413 | Always/Tampax bladder supports | Procter & Gamble | 2015 | — |
| 0 (this device) | K183468 | Revive Reusable Bladder Support | Rinovum Subsidiary 2, LLC | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 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 HHW? 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 HHW device
- #1 K253698 Milex™ Incontinence Dish Pessaries; Milex™…score 11.0 · 2 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 |
|---|---|---|---|
| * | K151413 | Always/Tampax bladder supportsSummary page 4…trical/Gynecological • Device Class – 2 • Regulation Number – 21 CFR § 884.3575 Predicate Device Proctor & Gamble Always/Tampax bladder supports (K151413) Reference Device ConTIPI Ltd. Improve Bladder Supports (K131198) Rinovum Subsidiary 2, LLC Decembe… | 2015 |
| † | K131198 | Tipi Otc | 2013 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| May 2, 2019 | Class II | Z-1952-2019 | Process change control | The product is unable to meet the use life of 31 cycles and may split or crack at the base of the "petals" after repeated use but within the use life of the product (31 uses). |
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 7.2 years on median.
- None of the 5 ancestors has a recall.
How does its category compare?
All HHW devicesHHW Pessary, Vaginal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · HHW
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HHW
263in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HHW
1in 2015
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HHW
39in 2025
MAUDE reports naming product code HHW, 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 | 4 |
| 2008 | 1 | — | 0 | 2 |
| 2009 | 1 | — | 0 | 2 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 1 |
| 2012 | 0 | — | 0 | 2 |
| 2013 | 1 | — | 9 | 0 |
| 2014 | 2 | — | 2 | 5 |
| 2015 | 1 | — | 1 | 1 |
| 2016 | 1 | — | 0 | 6 |
| 2017 | 0 | — | 0 | 5 |
| 2018 | 1 | — | 0 | 3 |
| 2019 | 2 | — | 0 | 15 |
| 2020 | 0 | — | 0 | 401 |
| 2021 | 0 | — | 0 | 24 |
| 2022 | 0 | — | 0 | 14 |
| 2023 | 0 | — | 0 | 12 |
| 2024 | 5 | 263 | 0 | 6 |
| 2025 | 1 | — | 0 | 39 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Revive bladder support is intended for temporary management of urine leakage caused by stress urinary incontinence (SUI) in women, 18 years and older.
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/K183468 · printed Nov 6, 2026
Cite this page
510(k) Report. “K183468: Revive Reusable Bladder Support.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K183468
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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