WestRock Converting, LLC

FDA Device Registration & Listing · Knoxville, TN, US · Registration 3010041486

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
3010041486
FEI Number
3010041486
Entity Name
WestRock Converting, LLC
City/State/Country
Knoxville, TN, US
Establishment Address
440 Goodys Ln, Knoxville, TN 37922, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
WestRock Converting, LLC (Owner Number: 9056422)
Owner / Operator Contact Address
5950 Grassy Creek Blvd., Winston Salem, NC 27105, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN220078
PMA Number
N/A

All Registered Proprietary Names

THERMACARE Manual toothbrush Toothbrush, Manual

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2006-06-05
EFW Toothbrush, Manual Dental Class 1 872.6855 2003-09-08
QWW Non-Medicated Topical Formulation For Treatment Of Erectile Dysfunction. Gastroenterology, Urology Class 2 876.5021 2024-09-09

Official Correspondent

Craig Smith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WestRock Converting, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008366788 WestRock Converting Company Lithia Springs, GA, US
3027909953 WESTROCK CONVERTING, LLC York, PA, US
3005607112 WestRock Converting, LLC RIDGEWAY, VA, US
3004134939 WestRock Converting, LLC Winston Salem, NC, US
3004270595 WESTROCK CONVERTING, LLC BOLINGBROOK, IL, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010041486. Last updated year: 2026. Please use registration number 3010041486 when referencing this establishment in official correspondence.
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