510(k) · Cleared
ClearedUrgent PC Neuromodulation System, Models UPC200 and UPC250-12
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Uroplasty, Inc. · NAM Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence
Cleared on Aug 20, 2007 as substantially equivalent to K061333 (Uroplasty, Inc., 2006) after a 48-day review. Its family tree reaches back 2 generations to 2005. 4 later devices descend from it.
- Decided
- Aug 20, 2007
- Review
- 48 days
- Class
- Class II
- Product code
- NAM
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K052025 (2005). 4 later devices descend from it, 2 citing it directly.
- Root · 2 generations backK052025 Urgent PC Neuromodulation SystemUroplasty, Inc. · 2005
- 1 generation backK061333 Urgent PC Neuromodulation System, Models UPC200-a and UPC250-12Uroplasty, Inc. · 2006
- This deviceK071822 Urgent PC Neuromodulation System, Models UPC200 and UPC250-12Uroplasty, Inc. · 2007
- Descendant · cites it directly · 1 of its ownK192731 ZIDA Wearable Neuromodulation SystemExodus Innovations · 2021
- Descendant · cites it directly · 1 of its ownK101847 Urgent PC Stimulator; Urgent PC Lead SetUroplasty, Inc. · 2010
- Descendant · 2 generations on · 0 of its ownK220454 Vivally System Wearable, Non-Invasive Neuromodulation System and…Avation Medical, Inc. · 2023
- Descendant · 2 generations on · 0 of its ownK132561 Nuro Neuromodulation SystemAdvanced Uro-Solutions, Inc. · 2013
Most influential descendants
Showing 4 of 4 · See all- K192731ZIDA Wearable Neuromodulation SystemExodus Innovations · 2021 · cites it directly1descendant
- K101847Urgent PC Stimulator; Urgent PC Lead SetUroplasty, Inc. · 2010 · cites it directly1descendant
- K220454Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile ApplicationAvation Medical, Inc. · 2023 · 2 generations on0descendants
- K132561Nuro Neuromodulation SystemAdvanced Uro-Solutions, Inc. · 2013 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K052025 | Urgent PC Neuromodulation System | Uroplasty, Inc. | 2005 | — |
| −1 | K061333 | Urgent PC Neuromodulation System, Models UPC200-a and UPC250-12 | Uroplasty, Inc. | 2006 | — |
| 0 (this device) | K071822 | Urgent PC Neuromodulation System, Models UPC200 and UPC250-12 | Uroplasty, Inc. | 2007 | — |
| +1 | K192731 | ZIDA Wearable Neuromodulation System | Exodus Innovations | 2021 | — |
| +1 | K101847 | Urgent PC Stimulator; Urgent PC Lead Set | Uroplasty, Inc. | 2010 | — |
| +2 | K220454 | Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile… | Avation Medical, Inc. | 2023 | — |
| +2 | K132561 | Nuro Neuromodulation System | Advanced Uro-Solutions, Inc. | 2013 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
| 2013 | 1 | 0 |
| 2021 | 1 | 0 |
| 2023 | 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 NAM? 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 NAM device
- #1 K220454 Vivally System Wearable, Non-Invasive…score 6.0 · 4 generations · no Class I recall
- #2 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 |
|---|---|---|---|
| * | K061333 | Urgent PC Neuromodulation System, Models UPC200-a and UPC250-12Summary page 1…AUG 2 0 2007 New Device Name Urgent® PC Neuromodulation System Predicate Device Urgent® PC Neuromodulation System (K061333) Contact Uroplasty, Inc. 5420 Feltl Road Minnetonka, MN 55343… | 2006 |
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 2 years and passes through 1 company; a new generation was cleared every 1.1 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K192731 (Exodus Innovations, 2021) has gone furthest, with 1 descendant of its own.
How does its category compare?
All NAM devicesNAM Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · NAM
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · NAM
Too few NAM 510(k)s in any year since 2007 to give a median.
Recalls per year · NAM
No recall names NAM since 2007.
Adverse event reports per year · NAM
3in 2023
MAUDE reports naming product code NAM, 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 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 26 |
| 2017 | 0 | — | 0 | 52 |
| 2018 | 0 | — | 0 | 4 |
| 2019 | 0 | — | 0 | 2 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 2 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 1 | — | 0 | 3 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Urgent PC Neuromodulation System is intended to treat patients suffering from urinary urgency, urinary frequency, and urge incontinence.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K071822 · printed Nov 4, 2026
Cite this page
510(k) Report. “K071822: Urgent PC Neuromodulation System, Models UPC200 and UPC250-12.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071822
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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