Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005423373

FEI Number

3005423373

Entity Name

TRI-FI KNITTING, LLC

City/State/Country

Dunlap, TN, US

Establishment Address

2353 Lower East Valley Road, Dunlap, TN 37327, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

TRI-FI KNITTING, LLC (Owner Number: 9078919)

Owner / Operator Contact Address

2353 Lower East Valley Road, Dunlap, TN 37327, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KNITTED ELASTIC NET AND GAUZE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2005-10-25

Official Correspondent

Robert FLEMING JR

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TRI-FI KNITTING, 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 3005423373. Last updated year: 2026. Please use registration number 3005423373 when referencing this establishment in official correspondence.