SPECTRON IR

FDA Device Registration & Listing · Medford, OR, US · Registration 3007010903

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
3007010903
FEI Number
3007010903
Entity Name
SPECTRON IR
City/State/Country
Medford, OR, US
Establishment Address
841 W Stewart Ave Ste 9, Medford, OR 97501, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Spectron IR (Owner Number: 10028874)
Owner / Operator Contact Address
841 W Stewart Ave #9, Medford, OR 97501, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K023434
PMA Number
N/A

All Registered Proprietary Names

Spectron IR Spectrum 9000 MB

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 2011-04-08
LHQ System, Telethermographic (Adjunctive Use) Obstetrics/Gynecology Class 1 884.2980 2014-03-17

Official Correspondent

Thomas Crandall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Spectron IR
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 3007010903. Last updated year: 2026. Please use registration number 3007010903 when referencing this establishment in official correspondence.
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