Data / Medical devices / United States / Neux Technologies, Inc.
Neux Technologies, Inc.: FDA-registered device maker in Tampa, FL, United States, 1 510(k) clearance
Neux Technologies, Inc. is registered with the FDA (registration 3017146742) in Tampa, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 11, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017146742
- Address
- 802 E Whiting Street, Tampa, FL, United States, 33602
- Owner or operator
- NeuX Technologies, Inc. (10076258)
- Roles
- Specification developer
- First device listed
- July 13, 2020
- Registered through
- 2026
- Brand names listed
- Interactive Neuromuscular Stimulation, NXPro, NeuX, iNMS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | 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 |
|---|---|---|---|---|---|---|
| October 11, 2019 | K191181 | NXPRO Neuromuscular Electrical Stimulation Device | NGX | Substantially Equivalent | Neux Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 11, 2019. 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.