Data / Medical devices / United States / InterX Technologies
InterX Technologies: FDA-registered device maker in Plano, TX, United States, 4 510(k) clearances
InterX Technologies is registered with the FDA (registration 3004786509) in Plano, TX, United States. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 21, 2013. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004786509
- Address
- 3465 Technology Dr., Suite A, Plano, TX, United States, 75074
- Owner or operator
- InterX Technologies (10051305)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- March 1, 2016
- Registered through
- 2026
- Brand names listed
- InterX 1000/Derma 200 Stimulator For Cosmetic Use, InterX Self-Adhesive Dual Electrode - Non-Sterile, InterX500 Flexible Array Electrode, InterX5000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Manufacturer, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| June 21, 2013 | K130816 | INTERX STERILE SELF-ADHESIVE DUAL ELECTRODE (ISSDE) | GXY | Substantially Equivalent | Neuro Resource Group, Inc. | accessdata.fda.gov |
| April 4, 2008 | K070217 | INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE | NFO | Substantially Equivalent | Neuro Resource Group, Inc. | accessdata.fda.gov |
| March 29, 2006 | K053626 | INTERX500 FLEXIBLE ARRAY ELECTRODE | GXY | Substantially Equivalent | Neuro Resource Group, Inc. | accessdata.fda.gov |
| May 17, 2005 | K042912 | INTERX5000 | GZJ | Substantially Equivalent | Neuro Resource Group, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| February 7, 2011 | 58255 | Not yet classified | Terminated | Inter x 5002 Device, Inter x Professional Sport Device, Inter x 1000 Personal Device, and Inter x Personal Sport packaged with Triad alcohol wipes. The alcohol wipes manufactured by the Triad Group were labeled under bra | Product package contains alcohol prep pads recalled by Triad Group because the prep pads have the potential to be contaminated with an objectionable organism. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Electrode, Cutaneous
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Updated June 21, 2013. 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.