Data / Medical devices / Stimulator, Transcutaneous Electrical, Aesthetic Purposes / United States
FDA-registered makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Stimulator, Transcutaneous Electrical, Aesthetic Purposes (product code NFO). 13 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- Product code
- NFO
- Country
- United States
Makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Carol Cole Company dba NuFACE | Vista, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 12 | June 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| Micro Current Technology, Inc. | Seattle, WA, United States | Manufacturer, Repackager or relabeler | 4 | July 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Xtreem Pulse | New York, NY, United States | Manufacturer, Specification developer | 4 | March 6, 2025 | 0 | 0 | 0 | api.fda.gov |
| A-1 Engineering | Irvine, CA, United States | Manufacturer | 1 | September 3, 2025 | 0 | 0 | 0 | api.fda.gov |
| Alc Enterprises Inc | Brooklyn, NY, United States | Specification developer | 1 | December 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Avazzia, Inc. | Dallas, TX, United States | Manufacturer | 1 | April 27, 2021 | 0 | 0 | 0 | api.fda.gov |
| Biosonic Technologies, LLC | Las Vegas, NV, United States | Specification developer | 1 | April 30, 2014 | 0 | 0 | 0 | api.fda.gov |
| Heat In A Click LLC | Dania, FL, United States | Specification developer | 1 | April 26, 2018 | 0 | 0 | 0 | api.fda.gov |
| InterX Technologies | Plano, TX, United States | Manufacturer, Repackager or relabeler | 1 | April 4, 2008 | 0 | 0 | 0 | api.fda.gov |
| Nse Products, Inc. | Provo, UT, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | November 21, 2023 | 0 | 0 | 0 | api.fda.gov |
| Raja Trading Company, Inc. | Fairfax, VA, United States | Manufacturer, Repackager or relabeler | 1 | February 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 1 | September 29, 2021 | 0 | 0 | 0 | api.fda.gov |
| Ziip Inc | Concord, CA, United States | Manufacturer | 1 | September 23, 2021 | 0 | 0 | 0 | api.fda.gov |
| Clarity Design, Inc. | Poway, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mendell | Lakeville, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Svtronics, Inc. | Plano, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.