Data / Medical devices / United States / Iq Technologies Inc.
Iq Technologies Inc.: FDA-registered device maker in Las Vegas, NV, United States, 1 510(k) clearance
Iq Technologies Inc. is registered with the FDA (registration 3008806536) in Las Vegas, NV, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 6, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008806536
- Address
- 4731 West Post Road Suite 130, Las Vegas, NV, United States, 89119
- Owner or operator
- IQ Technologies Inc. (10035251)
- Roles
- Repackager or relabeler
- First device listed
- November 23, 2015
- Registered through
- 2026
- Brand names listed
- EMS, IQ massage chairs, IQSkyline massage chairs, Stimulator, TENS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | 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 |
|---|---|---|---|---|---|---|
| August 6, 2014 | K131290 | IQ TECHNOLOGIES | NUH | Substantially Equivalent | Iq Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated August 6, 2014. 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.