WESTROCK CONVERTING, LLC

FDA Device Registration & Listing · York, PA, US · Registration 3027909953

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
3027909953
FEI Number
3027909953
Entity Name
WESTROCK CONVERTING, LLC
City/State/Country
York, PA, US
Establishment Address
115 Willow Springs LN, York, PA 17406, 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
N/A
PMA Number
N/A

All Registered Proprietary Names

Poligrip Partials; Super Polygrip Cream; Super Poligrip Cushion & Comfort; Super Poligrip Powder Artificial Saliva Biotene mouth spray Biotene Dry Mouth Gentle Oral Rinse Gentle Mint; Biotene Moisturizing Spray; Biotene Oral Balance Gel Poligrip Cushion Comfort; Poligrip Max Seal Denture Adhesive; Poligrip Super Denture Adhesive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KOT Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium Dental Class 1 872.3490 2023-10-13
LFD Saliva, Artificial Unknown Class U N/A 2023-10-13
LFD Saliva, Artificial Unknown Class U N/A 2023-10-13
LFD Saliva, Artificial Unknown Class U N/A 2023-10-13
KOL Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer Dental Class 1 872.3410 2023-10-13

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
3005607112 WestRock Converting, LLC RIDGEWAY, VA, US
3004134939 WestRock Converting, LLC Winston Salem, NC, US
3010041486 WestRock Converting, LLC Knoxville, TN, US
3004270595 WESTROCK CONVERTING, LLC BOLINGBROOK, IL, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K884357 Precision Dynamics Corp. PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM 1988-11-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027909953. Last updated year: 2026. Please use registration number 3027909953 when referencing this establishment in official correspondence.
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