Data / Medical devices / System, Telethermographic (Adjunctive Use) / United States
FDA-registered makers of System, Telethermographic (Adjunctive Use) in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make System, Telethermographic (Adjunctive Use) (product code LHQ). 7 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- System, Telethermographic (Adjunctive Use)
- Product code
- LHQ
- Country
- United States
Makers of System, Telethermographic (Adjunctive Use) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Spectron Ir | Medford, OR, United States | Manufacturer | 2 | October 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| Infrared Cameras Inc. | Beaumont, TX, United States | Manufacturer | 1 | July 11, 2008 | 0 | 0 | 0 | api.fda.gov |
| Med-Hot Thermal Imaging, Inc | Lakeland, FL, United States | Manufacturer | 1 | December 8, 2017 | 0 | 1 | 0 | api.fda.gov |
| Meditherm Inc. | Albuquerque, NM, United States | Manufacturer | 1 | February 21, 2001 | 0 | 0 | 0 | api.fda.gov |
| Titronics Research & Development | Tiffin, IA, United States | Manufacturer | 1 | October 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| Ue Lifesciences Inc. | Philadelphia, PA, United States | Specification developer | 1 | February 10, 2012 | 0 | 0 | 0 | api.fda.gov |
| USA Therm Inc. | Hollywood, FL, United States | Specification developer | 1 | September 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| Design Catapult Manufacturing | Fountain Valley, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.