Data / Medical devices / United States / USA Therm Inc.
USA Therm Inc.: FDA-registered device maker in Hollywood, FL, United States, 1 510(k) clearance
USA Therm Inc. is registered with the FDA (registration 3041915306) in Hollywood, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 14, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3041915306
- Address
- 2031 Harrison Street Suite #7, Hollywood, FL, United States, 33020
- Owner or operator
- USA Therm, Inc. (10094440)
- Roles
- Specification developer
- First device listed
- November 30, 2025
- Registered through
- 2026
- Brand names listed
- ThermPix
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Telethermographic (Adjunctive Use) | LHQ | 1 | 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 |
|---|---|---|---|---|---|---|
| September 14, 2023 | K232462 | ThermPix Thermovisual Camera | LHQ | Substantially Equivalent | Usa Therm, Inc. | accessdata.fda.gov |
Compare with other makers
Updated September 14, 2023. 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.