Data / Medical devices / United States / Titronics Research & Development
Titronics Research & Development: FDA-registered device maker in Tiffin, IA, United States, 1 510(k) clearance
Titronics Research & Development is registered with the FDA (registration 1933956) in Tiffin, IA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 10, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1933956
- FEI number
- 3001451268
- Address
- 400 Stephans Street, Suite D Box 470, Tiffin, IA, United States, 52340
- Owner or operator
- TITRONICS RESEARCH & (9032132)
- Roles
- Manufacturer
- First device listed
- December 14, 2007
- Registered through
- 2026
- Brand names listed
- C-5000, TYTRON RANGE OF MOTION DEVICE, Tytron C-5000, Tytron C-500IR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Goniometer, Ac-Powered | KQX | 1 | Manufacturer | accessdata.fda.gov |
| System, Telethermographic (Adjunctive Use) | LHQ | 1 | Manufacturer | accessdata.fda.gov |
| Thermometer, Clinical Color Change | FQZ | 1 | 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 |
|---|---|---|---|---|---|---|
| October 10, 2003 | K032471 | TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM | LHQ | Substantially Equivalent | Titronics Research & Development Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Goniometer, Ac-Powered
- All makers of Thermometer, Clinical Color Change
- All makers of System, Telethermographic (Adjunctive Use)
Updated October 10, 2003. 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.