Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017728970

FEI Number

3017728970

Entity Name

TENNESSEE FOAM, LLC

City/State/Country

Knoxville, TN, US

Establishment Address

910 Callahan Dr. Ste 108, Knoxville, TN 37912, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Tennessee Foam, LLC (Owner Number: 10083505)

Owner / Operator Contact Address

910 Callahan Dr. Ste 108, Knoxville, TN 37912, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GRI-Alleset GRI-Alleset, Inc.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMP	Cushion, Wheelchair	Physical Medicine	Class 1	890.3920	2021-11-25
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2022-01-25

Official Correspondent

Martin Paugh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tennessee Foam, LLC

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 3017728970. Last updated year: 2026. Please use registration number 3017728970 when referencing this establishment in official correspondence.