Data / Medical devices / Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence
Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence (NAM): 7 FDA-registered makers in 2 countries
7 establishments in 2 countries are registered with the FDA to make Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence (product code NAM, Class 2, 21 CFR 876.5310). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on April 3, 2023, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- NAM
- Device class
- 2
- Regulation
- 876.5310
- Medical specialty
- Gastroenterology, Urology
Makers by country
| Country | Makers |
|---|---|
| United States | 6 |
| Israel | 1 |
Makers of Stimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avation Medical | Valencia, CA, United States | Manufacturer | 1 | April 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Exodus Innovations | Sufa Southern, Israel | Manufacturer | 1 | March 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Neuromodulation | Minneapolis, MN, United States | Manufacturer | 1 | November 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| Uroplasty, LLC | Minnetonka, MN, United States | Manufacturer, Specification developer | 1 | October 21, 2010 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Wabasha, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nortech Systems, Inc. | Milaca, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Tech Services, LLC | Bloomington, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated April 3, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.