Data / Medical devices / United States / Nse Products, Inc.
Nse Products, Inc.: FDA-registered device maker in Provo, UT, United States, 2 510(k) clearances
Nse Products, Inc. is registered with the FDA (registration 3001236514) in Provo, UT, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 21, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001236514
- Address
- 75 W Center St, Provo, UT, United States, 84601
- Owner or operator
- NSE Products, Inc. (10047214)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- July 21, 2014
- Registered through
- 2026
- Brand names listed
- AP 24 Smile Pop, Conductive Gel, RenuSpa iO
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Media, Electroconductive | GYB | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 21, 2023 | K232001 | Nu Skin RenuSpa iO | NFO | Substantially Equivalent | Nse Products, Inc. | accessdata.fda.gov |
| September 13, 2002 | K022006 | CONDUCTIVE GEL | GYB | Substantially Equivalent | The Dezac Group | accessdata.fda.gov |
Compare with other makers
- All makers of Toothbrush, Manual
- All makers of Media, Electroconductive
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Updated November 21, 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.