Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010873607

FEI Number

3010873607

Entity Name

CHEMVIRON CARBON

City/State/Country

Houghton le Spring England, GB

Establishment Address

Rainton Bridge Industrial Estate, Houghton le Spring England DH4 5PP, GB

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Chemviron Carbon (Owner Number: 10046659)

Owner / Operator Contact Address

Chemviron Carbon Cloth Division, Rainton Bridge Industrial Estate, Houghton le Spring, GB-ENG DH4 5PP, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Zorflex Zorflex LA Zorflex VB-K

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2014-04-23

Official Correspondent

Mark Reynolds

US Agent Details

Samuel Yates Business: Calgon Carbon Corporation Email: samuel.yates@kuraray.com Phone: (412) 4199926

Related Public Records

Same Entity

Chemviron Carbon

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 3010873607. Last updated year: 2026. Please use registration number 3010873607 when referencing this establishment in official correspondence.