Titronics Research & Development

FDA Device Registration & Listing · TIFFIN, IA, US · Registration 1933956

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1933956
FEI Number
3001451268
Entity Name
Titronics Research & Development
City/State/Country
TIFFIN, IA, US
Establishment Address
400 Stephans Street, Suite D Box 470, TIFFIN, IA 52340, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TITRONICS RESEARCH & (Owner Number: 9032132)
Owner / Operator Contact Address
400 STEPHANS STREET, STE D Box 470, Tiffin, IA 52340, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tytron C-500IR C-5000 Tytron C-5000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LHQ System, Telethermographic (Adjunctive Use) Obstetrics/Gynecology Class 1 884.2980 2007-12-14
FQZ Thermometer, Clinical Color Change General Hospital Class 1 880.2900 2023-12-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TITRONICS RESEARCH &
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1933956. Last updated year: 2026. Please use registration number 1933956 when referencing this establishment in official correspondence.
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