Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008190709

FEI Number

3008190709

Entity Name

Renfro LLC

City/State/Country

Cleveland, TN, US

Establishment Address

4405 Michigan Avenue Rd NE, Cleveland, TN 37323, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

RENFRO LLC (Owner Number: 9068158)

Owner / Operator Contact Address

661 Linville Road, --, Mount Airy, NC 27030, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dr. Scholl's

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQL	Stocking, Medical Support (For General Medical Purposes)	General Hospital	Class 1	880.5780	2004-11-12

Official Correspondent

Todd Roeder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RENFRO 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 3008190709. Last updated year: 2026. Please use registration number 3008190709 when referencing this establishment in official correspondence.