Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1062620

FEI Number

3001237189

Entity Name

SANDERS MEDICAL PRODUCTS, INC.

City/State/Country

KNOXVILLE, TN, US

Establishment Address

10475 Dutchtown Rd, KNOXVILLE, TN 37932, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SANDERS MEDICAL PRODUCTS, INC. (Owner Number: 9031573)

Owner / Operator Contact Address

10475 Dutchtown Road, --, Knoxville, TN 37932, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Line Source Rod Source Uniform Phantom

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IXD	Source, Calibration, Sealed, Nuclear	Radiology	Class 1	892.1400	1997-09-15
IYQ	Phantom, Flood Source, Nuclear	Radiology	Class 1	892.1380	1997-09-15

Official Correspondent

JOHN SANDERS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SANDERS MEDICAL PRODUCTS, INC.

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 1062620. Last updated year: 2026. Please use registration number 1062620 when referencing this establishment in official correspondence.