Data / Medical devices / United States / International Health Technologies
International Health Technologies: FDA-registered device maker in Salt Lake City, UT, United States, 3 510(k) clearances
International Health Technologies is registered with the FDA (registration 3010078139) in Salt Lake City, UT, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 13, 2006. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3010078139
- Address
- 2355 So. 1070 W. Ste. D, Salt Lake City, UT, United States, 84119
- Owner or operator
- International Health Technologies (10044346)
- Roles
- Manufacturer
- First device listed
- May 29, 2013
- Registered through
- 2026
- Brand names listed
- BioScan, BioScan Gen ii, Bioscan, MSA21, MSAS Professional, Nano SRT, Vantage, VantagePro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Biofeedback | HCC | 2 | Manufacturer | accessdata.fda.gov |
| Device, Galvanic Skin Response Measurement | GZO | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 13, 2006 | K053004 | MSAS-VANTAGE | GZO | Substantially Equivalent | Biomeridian, Int. | accessdata.fda.gov |
| January 20, 2000 | K993824 | MSAS PROFESSIONAL | GZO | Substantially Equivalent | Biomeridian, Int. | accessdata.fda.gov |
| March 14, 1996 | K924313 | DIGITAL CONDUCTANCE METER | HCC | Substantially Equivalent | The Jayms Co. | accessdata.fda.gov |
Compare with other makers
Updated January 13, 2006. 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.